Oh sentence example

oh
  • Oh, I forgot to ask.
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  • Oh, what a pretty sound it made!
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  • "Oh my gosh!" she said, looking back at the photo to read the statistics.
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  • Oh yes, very much.
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  • Oh! he muttered, looking down from the window at the stones of the pavement.
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  • Oh, and they change color if they detect structural weakness in the material to which they are affixed.
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  • Oh, but he must be.
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  • Oh, I'd love to come here and fish sometime.
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  • "Oh, I believe you," Claudette interrupted flippantly.
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  • Oh, I don't know.
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  • Oh, what has happened?
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  • Oh, he told me part of his plans, all right.
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  • Oh, you little ones; be careful and don't talk to strangers!
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  • Oh, how you have...
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  • Oh. Well, why don't you go with me then?
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  • Oh, what's the use?
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  • "Oh, I forgot to tell you," he said.
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  • Oh, I'm a Wizard; you may be sure of that.
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  • "Oh, no!" said another man who had seen and heard it all.
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  • So when I knocked on the door of Jim's atelier and said, "Hey, I'm Byron Reese," he said, "Oh, Byron, come over here, I want you to meet this guy.
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  • "Oh no, not at all too young!" replied the count.
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  • Oh, he's not mean.
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  • "Oh God," she cried softly.
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  • "Oh, you're in a library," he said.
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  • Oh, it was all so interesting, so beautiful!
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  • "Oh, very interesting!" said Mademoiselle Bourienne.
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  • Oh, you think Alex feels like you want his attention all the time?
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  • "Oh," he said, smiling.
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  • "Oh," Davis interrupted, raising his brows.
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  • "Oh, no," answered the Sawhorse.
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  • Oh, do you know?
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  • Oh, I guess I am a little sleepy.
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  • "Oh, cut it short," said Eureka; "you've talked long enough."
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  • Oh, and they are smart nails.
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  • Oh, the delight with which I gathered up the fruit in my pinafore, pressed my face against the smooth cheeks of the apples, still warm from the sun, and skipped back to the house!
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  • Oh, Carrie, how I should like to speak like other people!
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  • And oh, the housekeeping! to keep bright the devil's door-knobs, and scour his tubs this bright day!
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  • Oh, they swarm; the sun is too warm there; they are born too far into life for me.
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  • Oh, how happy I am!
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  • Oh, I was supposed to tell you about a party.
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  • Oh, I was going to ask you.
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  • Oh, we disagree now and then, but we never come to blows.
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  • "Oh, god!" she gasped.
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  • Oh God, I'm going crazy!
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  • N: C OH, CH: N O, C: N OH.
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  • Ag ?HC 'OH ?H CO 2 H-f-H 2 N OH, and also on the production from sodium nitromethane and mercuric chloride, thus CH 2: NO Ohg - > H 2 O -I-C: NOhg (hg = 2 Hg).
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  • ethylene dibromide) with silver acetate or with potassium acetate and alcohol, the esters so produced being then hydrolysed with caustic alkalis, thus: C 2 H 4 Br 2 + C2H302 Ag-*C2H4(O C2H30)2->C2H4(OH)2+2K C2H302 by the direct union of water with the alkylen oxides; by oxidation of the olefines with cold potassium permanganate solution (G.
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  • Glycols may be classified as primary, containing twoCH(OH groups; primary-secondary, containing the grouping - CH(OH) CH (OH; secondary, with the grouping - CH(OH) CH(OH) -; and tertiary, with the grouping > C (OH) (OH) C
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  • "Oh, I cannot hope ever to be like you," sighed the Sawhorse.
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  • "Oh, Edward, there is Mr. Harris!" whispered the little girl.
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  • "Oh, well," said the groom, "won't six nails do?
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  • "Oh, any kind of a place will suit him," answered the landlord.
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  • "Oh, I have a plan for making a boat move without poling it or rowing it," he answered.
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  • "Oh, that will be easy enough," was the answer.
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  • Oh, would that men would leave the city, its splendour and its tumult and its gold, and return to wood and field and simple, honest living!
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  • Oh, it was a lovely and delicate doll! but the little girl's brother, a tall lad, had taken the doll, and set it up in a high tree in the garden, and had run away.
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  • Oh, I do so hope and pray that I shall speak well some day!...
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  • Oh my! if they only realized their limitations, they would flee for their lives to the woods and fields.
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  • Oh, he was simply beautiful!
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  • We dined with the Rogers last Friday, and oh, they were so kind to us!
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  • Oh, if only there were some one to help me!
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  • Oh dear, what am I thinking about?
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  • Oh! she heard as she left the room.
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  • "Oh, how delightful it is!" she kept saying, running up to Sonya.
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  • Oh, how pleasant it was at home!...
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  • "Oh dear, what a young lady!" said Foka, pretending to frown at Natasha.
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  • Oh, that this toil might end and you would release me! thought he.
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  • "Oh come, that's enough!" said the other.
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  • "Oh, if anyone knew how little anything matters to me now," she said.
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  • Oh yes, an artful tale!
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  • Oh well, there are always others.
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  • Oh, and tell him I swear not to look at what other girl's he's been calling... cross my heart, like fun!
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  • "Oh, god!" she said, flopping down on the sofa and looking up the stairs.
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  • Oh, I left the phone off the hook.
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  • I'm more used to country property where doors and windows are left open, making my life oh so easy.
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  • "Oh God, I hate myself," she said through her tears.
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  • "Oh, you must mean Mr. Green, in the Pace Arrow," the woman said.
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  • All I could think was once again, we were oh so close, but he'd alluded us.
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  • Oh, do I have Mr. Abbott?
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  • "Oh, wait, don't shut the-- " The door to the apartment clicked shut, locking automatically.
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  • Oh, and the devil.
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  • Oh, and the tropical storm will become a hurricane late Saturday night.
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  • "Oh, it is," Toni replied with a wink.
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  • Oh, and I found where I think the lab was.
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  • "Uh oh," Darian whispered.
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  • Oh, and I look forward to kicking his ass.
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  • Oh, and bring your things.
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  • "Oh, Sean," she said with a smile.
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  • "Oh, here," she said and reached for her purse.
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  • Oh, and not run me over?
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  • "Oh my God," she whispered.
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  • Oh, God, what's wrong now?
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  • You'd think after oh, a few thousand years, you'd remember, Jule.
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  • Oh, ye of little faith, he said into her mind.
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  • "Oh, god," she breathed.
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  • "Oh, god," she mumbled with a look at Darkyn.
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  • Oh, to have had this instinct years ago, when she met Wynn!
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  • "Oh, god, Gabriel," she whispered, stricken.
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  • Oh, shit was all Dean could think, but he willed the words to stay put.
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  • Oh, no you don't!
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  • Oh, I think you can trust her—on this business.
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  • "Oh, no," Deidre mumbled.
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  • "Oh, no, I don't want that one," she objected and pulled out a sweater.
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  • "Oh, only my soul," she replied with a half-laugh.
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  • "Oh my god!" she exclaimed.
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  • "Oh!" she exclaimed, her amethyst eyes unusually large.
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  • "Oh God, Alex," she groaned.
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  • Oh, I was supposed to tell you.
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  • Oh yes, he started that last night.
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  • "Oh Alex," she moaned.
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  • Oh Alex, Mom and Dad would have loved this.
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  • Oh no, not bears.
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  • Oh, do they have chitterlings and hog jowls there?
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  • "Oh, no," she told him.
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  • "Oh, you don't want to know," she said with a sigh.
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  • "Oh, yeah," Gabe smiled.
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  • "Oh, god, Logan," she breathed, eyes watering.
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  • "Oh, Logan," she breathed then rushed on.
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  • Oh. You couldn't tell me?
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  • Oh, and stop calling me Doc.
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  • "Oh, god," she said, shuddering.
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  • "Oh, god," she said in embarrassment.
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  • "Oh, god!" she groaned.
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  • "How do you … oh, god," she whispered.
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  • Oh, and I picked up someone else's soul last night, she said.
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  • Oh. How do people mess with you?
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  • Oh, god, have I put him in danger?
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  • "Oh, god, what did you do to me this time?" she asked, grappling with fuzzy memories.
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  • "Oh, hell no," she said with a smile.
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  • "Oh, hon, I'm sorry to hear that," her sis said in a distracted tone that said she really didn't care.
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  • Oh, and wear something decent this time.
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  • "Oh, no!" he said with a laugh.
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  • Nope. Oh, but you might want to get some…Gabriel, what does he like?
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  • "Oh, no," she said, realizing his meaning.
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  • "Oh, now you give a damn!" she snapped, backing away.
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  • Oh no you don't!
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  • "Oh, god, Katie…" His voice was hoarse, a mix of pleasure and horror.
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  • Oh, god, Ully, this smells like a skunk crawled into my clothes!
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  • Oh. You.ve got, um, work?
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  • Oh, God, Jade, what did you do?
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  • "Oh, my," Jared said.
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  • Oh. I think I.ve heard his name before.
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  • Oh, the sweet smell of—
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  • "Oh, thank God!" she said with a deep sigh.
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  • "Oh, but wait!" she exclaimed.
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  • "Oh, damn you," she muttered, irritated her first sale was a pity sale and yet thinking even better of Romas for supporting his fiancée's hopeless friend.
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  • How did you tell your best friend that aliens were real and oh, by the way, I married one and am taking you with me to his planet, for your own good?
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  • I'm sure there will be someone-- oh, hell, don't look down!
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  • "Oh, nothing," Kiera lied.
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  • To her surprise, Evelyn stiffened and gave an oh-so-casual, "Oh?"
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  • Oh, and you may need one of these.
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  • Oh, I'm sure she was here!
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  • Oh, that's a shame!
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  • Oh, not so much.
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  • Oh, I knew he just thought that way because I was his kid, but I figured he was a pretty smart guy himself so he couldn't be all wrong.
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  • Oh, I guess I'm just being foolish like Claire says.
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  • The heat has been lowered now that the men have left and it is oh so cold as I lay huddled here beneath my thin blankets.
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  • And, oh so many more people on the streets!
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  • Oh, he said he'd take care of everything.
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  • Oh, he just follows the code and transcribes the letters.
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  • "Oh, she said, rubbing the sleep from her eyes, "I thought Mrs. Shipton was back."
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  • Oh, they can't be serious!
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  • "Oh, that one," Fred said, realizing Effie was perpetuating the misinformation about Annie Quincy's past, creating Annie the prostitute as a salvageable soul of Reverend and Mrs. Martin, a separate person from the true Boston ancestor.
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  • Oh, she empathizes with what they did.
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  • Oh, I'm right about it.
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  • "Oh yeah," she readily responded.
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  • Oh my, that feels wonderful.
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  • Claudia swallowed hard and whispered, "Oh yes."
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  • Jackson began to recount the whole story and with all the "Oh my Gods!" and "You're kiddings!"
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  • Oh, I have friends here.
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  • Oh, I guess he thinks she'll be more comfortable in it.
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  • Oh, I better get moving.
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  • Oh, Sweetie, I'm sorry, I forgot about breakfast.
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  • Oh jeez, I'm sorry.
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  • Oh, I moved it.
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  • Oh no, it's not that at all!
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  • Oh, it's beautiful, you can see forever!
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  • Oh, I don't think so.
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  • Oh, no, I couldn't.
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  • Oh, it's not done yet, maybe next time.
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  • Oh yeah, she's coming for dinner.
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  • Oh yeah, tenderloin will work.
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  • Sarah argued, Oh, come on.
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  • Oh no, I don't have anything prepared.
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  • Oh my gosh, it's so late.
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  • Oh, sorry, does this bother you?
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  • Oh my, what did you do?
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  • Oh, yes I do.
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  • Oh, my mistake, I thought you told me red.
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  • Oh no, really, all I have to do tonight is put the dishes back in the caterer's boxes.
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  • "Oh, that's heaven," she purred, as he massaged her feet and calves.
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  • Oh yeah, I hate that, it hurts.
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  • Oh Jackson, it was wonderful.
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  • Oh, that will be nice.
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  • Oh, man, that's tough.
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  • Oh, I love presents.
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  • Oh my God, it's perfect.
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  • Oh God, no, I want you here with me, don't even think about leaving, please.
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  • Oh God, where is she now?
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  • Oh, Mr. Jackson, I hear you're not feeling well.
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  • Oh yeah, I need to get some air.
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  • Oh, I put that in the closet.
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  • Oh, I'm guest lecturing at Rhode Island School of Design.
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  • She chuckled, Oh, I'm sorry.
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  • Oh, is that tonight?
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  • Oh yeah, for sure.
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  • Oh, Miss Sidwell, you have me quite smitten.
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  • Oh, we should get going then.
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  • Oh, it was wonderful.
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  • Jackson heard Elisabeth say, "Ouch. Oh no, I cut myself."
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  • Oh, no you don't, you give it up now.
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  • Oh girl, isn't the vamp sex the best?
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  • Oh, he'll be fine.
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  • Oh my, I guess I was pretty tired.
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  • Oh no, you didn't bring any blood?
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  • Oh, that's so exciting!
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  • Oh my God, she's really on your lap?
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  • Oh, that is an understatement.
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  • Oh, it's beautiful, congratulations.
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  • Oh Jackson, I love you so.
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  • Oh, no you don't, missy.
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  • Oh, I love you so!
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  • Oh, Mother, thank you so much.
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  • Oh, he'll have a fit or two and try to hand down an edict.
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  • Oh, Jackson, that's perfect!
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  • Oh, please sit with me.
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  • Oh, so you are still naive enough to hope he'll stick around.
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  • Oh, for heaven's sake, Carmen, they're goats, not race horses.
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  • Oh Carmen, just because he's wealthy doesn't mean he's a preppie.
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  • Oh, I wouldn't take it personally.
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  • Oh yes, with all the emergency supplies they had gathered for this occasion.
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  • Oh, there are a lot more breeds.
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  • Oh, give it a rest, Alex.
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  • Oh, don't worry about it.
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  • Oh, for heaven's sake, Katie.
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  • Oh, let's not talk about this right now.
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  • Oh Josh, get real.
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  • Oh well, now she'll have plenty of reason to kill off the mice.
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  • Oh, spring, hurry up.
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  • Oh, and that reminds me.
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  • Oh, if I only had a camera.
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  • Oh, come on Katie.
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  • Oh my gosh, Alex!
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  • Oh Alex, I can't help but wonder if some day when I'm bloated and cranky, you'll wish you hadn't given up your freedom.
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  • "Oh, God," she whispered.
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  • "Oh," she breathed, stopping midstride.
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  • Oh, yeah, that'll be fun.
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  • "Oh dear god," Dan said with a snort.
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  • Oh, because you Immortal jackasses know it all, right?
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  • Oh, no, Kris, you can't!
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  • "Oh, thank gods," Ully said from the cell across from Toby.
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  • He was an angel, and he wasn't her real nephew.  Oh, and they were in Hell.
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  • Oh, two, maybe three times a month.
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  • "Oh, no," Dean said.
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  • Oh, gee whiz, no.
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  • "Oh sure, Mr. Smith," the night manager grinned.
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  • "Oh," she said, sounding disappointed.
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  • Oh, he's a nice man too—he's in construction.
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  • "Oh, sure," she said sarcastically.
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  • "Oh," was all Dean could reply.
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  • Oh, like snooping—looking through my files.
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  • "Oh, sorry," Fred said.
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  • Oh, I guess I'd have gone back to being Mrs. Byrne—I'm too accommodating to have simply left him, and I do believe in my vows.
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  • Oh yes, that would make Lori a member of the Reynolds family too – technically.
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  • "Oh, I love number four," Joan broke in.
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  • Oh Carmen, you're 25, not 16.
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  • Oh, and Princess is seven months pregnant.
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  • Oh, I didn't know you were home yet.
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  • Oh my god, Carmen.
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  • Oh, so you got around it on a technicality.
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  • Oh. I'm glad you're putting something in your stomach.
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  • Oh, about how my life is changing.
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  • "Oh," She picked up the glass and sipped the sweet bubbly liquid.
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  • Oh, and it's not dangerous riding on the road?
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  • "Oh," she said with a sigh of relief.
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  • Oh, is that the game we were playing?
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  • Oh, I never noticed.
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  • "Oh," Carmen gasped, putting a hand to her mouth.
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  • Oh my gosh, Brutus!
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  • "Oh my gosh," she said, turning to look out the window.
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  • "Oh my gosh, Alex," she whispered.
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  • Oh, I believe your feelings for him are platonic.
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  • Oh, I've got the nerve.
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  • "Oh," Gerald said, "by the way, thanks for that financial advice.
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  • Oh, you cut me to the core.
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  • Oh, I almost forgot.
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  • Oh well, it would come some day, when the foal did something unusual.
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  • Oh yes, she had pneumonia.
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  • Oh yes you did.
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  • "Oh," her face grew warmer.
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  • Oh, yes, I'll kill as many as I can.
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  • "Oh, you mean this?" she asked with faux innocence.
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  • Oh, thank god, she said, sighing.
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  • Oh, and try to stay alive, she summarized.
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  • "Oh, he's not a vamp anymore," Yully said with her musical Irish lilt.
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  • Oh. He's here, but … no one else is, Darian.
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  • "Oh, we'll survive," he assured her.
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  • Oh Alex, I love you so much.
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  • Oh, then you and Josh never married?
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  • Oh, so he belongs to you.
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  • He paused and then added, "Oh, and my last name is Wilson."
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  • Oh, about 30 miles per hour.
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  • "Oh, that's why I came out here," he responded in a dry tone.
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  • Oh, I'd better call Felipa and tell her we'll meet them at the barn instead.
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  • Oh, you're awake now.
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  • Oh, we would not get lost.
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  • Oh, this would be an excellent idea!
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  • Oh for …He has a lot of room to talk.
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  • Oh, how she would love to be taken in his arms.
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  • Oh. I suppose the atmosphere is a little depressing around here right now.
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  • Oh Dad, I'm not a little girl any more.
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  • Oh yes - a new listing.
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  • "Oh nothing," Megan responded with a smile.
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  • Oh, I'll probably leave them up until the weather starts to get cold - unless someone objects, of course.
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  • Oh, I wouldn't worry.
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  • Oh, he was interested all right - interested in collecting the money offered to keep an eye on her.
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  • Oh, well enough, I suppose.
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  • Oh yes, the storm.
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  • Oh, you didn't have to do that.
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  • Oh, and a devastatingly handsome chicken farmer.
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  • Oh, he doesn't give me a chance to get lonely.
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  • Oh for heaven's sake, Dad.
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  • Oh, don't mind me.
    0
    0
  • Oh, for a telephone.
    0
    0
  • Oh, it feels so good.
    0
    0
  • Oh well, it'll do for a few weeks.
    0
    0
  • Oh, god, are you okay?
    0
    0
  • Oh, so you brought her here?
    0
    0
  • Oh. That's right you're a vampire.
    0
    0
  • I mean, he's got an incredible body, but … Oh, you're talking about sleeping with a different woman every night.
    0
    0
  • Oh, and tell Xander I'm not hitting on you.
    0
    0
  • "Oh, we haven't seen those yet," Toni said in a honeyed voice.
    0
    0
  • It's got like … oh, Ashley flushed.
    0
    0
  • Oh, now you want something from me, after threatening to take off my head?
    0
    0
  • Oh, yeah, I did.
    0
    0
  • "Oh, yes he is," Jessi said with a laugh that carried a hysterical edge.
    0
    0
  • Oh, she hasn't told you?
    0
    0
  • Oh, Brandon, is that why she hasn't dated since she took us in?
    0
    0
  • Grimaux by heating one part of glyoxylic acid with two parts of urea for ten hours at ioo° C.: 2CO(NH 2) 2 + CH(OH) 2 Oooh = 3h 2 O + C4H6N403.
    0
    0
  • PHARMACOSIDERITE, a mineral species consisting of hydrated basic ferric arsenate, 2FeAs04 Fe(OH)3.5H20.
    0
    0
  • Nef (1894), who proposed the formulae: C: N OH N: CH CH: N O C: N OH, O ?
    0
    0
  • Ethylene glycol, C2H4(OH)2, was first prepared by A.
    0
    0
  • a-propylene glycol, CH 3 CH(OH) CH 2 OH, a liquid boiling at 188° to 189°, and obtained by heating glycerin with sodium hydroxide and distilling the mixture; and trimethylene glycol, CH 2 OH CH 2 CH 2 OH, a liquid boiling at 214° C. and prepared by boiling trimethylene bromide with potash solution (A.
    0
    0
  • Cadmium hydroxide, Cd(OH) 2, is obtained as a white precipitate by adding potassium hydroxide to a solution of any soluble cadmium salt.
    0
    0
  • Nagel (Ber., 1898, 31, p. 2009), this oxide does not exist, the reaction leading to the formation of an hydroxide according to the equation: Mo 3 C1 4 (OH) 2 + 4KHO 3H 2 O = 3Mo(OH) 3 -l-4KBr+3H.
    0
    0
  • It is a yellow amorphous powder which is soluble in dilute alkalis, the solution on acidification giving an hydroxide, C1 4 Mo 3 (OH) 2, which is soluble in nitric acid, and does not give a reaction with silver nitrate.
    0
    0
  • Chromium oxychloride reacts violently on phenol, producing hydroquinone ether, O(C 6 H 4 OH)2; chromic acid gives phenoquinone, and potassium permanganate gives paradiphenol, oxalic acid, and some salicylic acid (R.
    0
    0
  • OH N (CH 3) 2 (i 3), are extensively employed in the manufacture of the important dyestuffs known as the rhodamines.
    0
    0
  • OH Nhch 3.
    0
    0
  • OH =S02C12+ H 2 SO It is a colourless fuming liquid which boils at 69° C. and which is readily decomposed by water into sulphuric and hydrochloric acids.
    0
    0
  • Fluorsulphonic acid, SO 2 F OH, is a mobile liquid obtained by the action of an excess of hydrofluoric acid on well-cooled sulphur trioxide.
    0
    0
  • OH, first prepared by A.
    0
    0
  • OH +PC1 5 = S 2 0 5 C1 2 + POC1 3 + 2HC1.
    0
    0
  • The acid is considered to possess the structure 0 2 S(SH) (OH), since sodium thiosulphate reacts with ethyl bromide to give sodium ethyl thiosulphate, which on treatment with barium chloride gives presumably barium ethyl thiosulphate.
    0
    0
  • Soc., 1902, 81, p. I) showed that this can be almost entirely avoided by replacing the manganese oxide by hydrated ferric oxide, the reaction proceeding according to the equation: 2Fe(OH) 3 3S0 2 = FeS 2 0 6 FeS0 3 3H 2 0.
    0
    0
  • AZURITE, or Chessylite, a mineral which is a basic copper carbonate, 2CuCO 3 Cu(OH) 2.
    0
    0
  • PHARAOH (Par`oh), the Hebraized title of the king of Egypt, in Egyptian Per-`o; Pheron in Herodotus represents the same.
    0
    0
  • yXvid r, sweet), a trihydric alcohol, trihydroxypropane, C 3 H 5 (OH) 3.
    0
    0
  • Berthelot, and many other chemists, from whose researches it results that glycerin is a trihydric alcohol indicated by the formula C 3 H 5 (OH) 3j the natural fats and oils, and the glycerides generally, being substances of the nature of compound esters formed from glycerin by the replacement of the hydrogen of the OH groups by the radicals of certain acids, called for that reason "fatty acids."
    0
    0
  • OH): The process of saponification may be viewed as the gradual progressive transformation of tristearin, or some analogously constituted substance, into distearin, monostearin and glycerin, or as the similar transformation of a substance analogous to distearin or to monostearin into glycerin.
    0
    0
  • 'CITRIC ACID,' Acidum citricum, or Oxytricarballylic Acid, C 3 H 4 (Oh) (Co.
    0
    0
  • Oh) 3, a tetrahydroxytribasic acid, first obtained in the solid state by Karl Wilhelm Scheele, in 1784, from the juice of lemons.
    0
    0
  • These discoveries of Geoffroy and Scheele formed the basis of Chevreul's researches by which he established the constitution of oils and the true nature of soap. In the article Oils it is pointed out that all fatty oils and fats are mixtures of glycerides, that is, of bodies related to the alcohol glycerin C 3H5(OH)3 i and some fatty acid such as palmitic acid (C 16 H 31 0 2)H.
    0
    0
  • Under suitable conditions C3H5(OH)3+3(C16H3102)H give C3H5(C16H3102)3+3H20 Glycerin.
    0
    0
  • But in this case the fatty acid unites with the alkali into its potash or soda salt, forming a soap C3H5(C16H3102)3+3NaOH =3NaC16H3102+C,H5(OH) 3 Palmitin.
    0
    0
  • Vogel, Jahresb., 18 53, p. 643), CS 2 -1-KHO+-R OH =H20+RO CS SK.
    0
    0
  • OH, whilst a strong reducing agent like hydriodic acid converts it into xanthene, the group >CO becoming > CH.
    0
    0
  • For instance, sulphuric acid is usually represented by the formula S0 2 (OH) 2, which indicates that it may be regarded as a compound of the group SO 2 with twice the group OH.
    0
    0
  • Groups of two or more atoms like SO 2 and OH, which are capable of playing the part of elementary atoms (that is to say, which can be transferred from compound to compound), are termed compound radicals, the elementary atoms being simple radicals.
    0
    0
  • It is convenient first to consider the effect of introducing one, two, or three hydroxyl (OH) groups into the - CH 3, > CH 2, and >CH groups, which we have seen to characterize the different types of hydrocarbons.
    0
    0
  • OH, >CH OH, and ?C OH; these compounds are known as alcohols (q.v.), and are termed primary, secondary, and tertiary respectively.
    0
    0
  • OH and >CH OH, with the production of radicals of the form - CH(OH) 2 and >C(OH)2.
    0
    0
  • A third hydroxyl group may be introduced into the - CH: 0 residue with the formation of the radical - C(OH) :0; this is known as the carboxyl group, and characterizes the organic acids.
    0
    0
  • Oxidation of thio-ethers results in the formation of sulphoxides, R2: S: 0, and sulphones, R2: S02; oxidation of mercaptans yields sulphonic acids, R S0 3 H, and of sodium mercaptides sulphinic acids, R S0(OH).
    0
    0
  • OH; R.CO Cl; (R.CO)20; R.CO SH; acid; acid-chloride; acid-anhydride; thio-acid; R CO NH 2 i R CO NH NH2.
    0
    0
  • The carbonyl oxygen may also be replaced by the oxime group,: N OH; thus the acids yield the hydroxamic acids, R C(OH): NOH, and the acid-amides the amidoximes, R C(NH 2): NOH.
    0
    0
  • The following diagrams illustrate these statements: - C ` H C OH HC /CH HC CH HC,/CH 'N/ HC CH CH CH From the benzene nucleus we can derive other aromatic nuclei, graphically represented by fusing two or more hexagons along common sides.
    0
    0
  • By fusing two nuclei we obtain the formula of naphthalene, C 1 oH 8; by fusing three, the hydrocarbons anthracene and phenanthrene, C14H10; by fusing four, chrysene, C18H12, and possibly pyrene, C16H1n; by fusing five, picene, C22 H 14.
    0
    0
  • OH, in which we will assume the hydroxyl group to occupy position I, is converted into brombenzene, which is then converted into benzoic acid, C 6 1-1 5 -COOH.
    0
    0
  • OH COOH, may be prepared; and the two other known oxybenzoic acids (ortho- and para-) may be converted into benzoic acid.
    0
    0
  • Certain a-diketones condense to form benzenoid quinones, two molecules of the diketone taking part in the reaction; thus diacetyl, CH 3 CO CO CH 3, yields p-xyloquinone, C 6 H 2 (CH 3) 2 0 2 (Ber., 1888, 21, p. 1411), and acetylpropionyl, CH 3 CO CO C 2 H 5, yields duroquinone, or tetramethylquinone, C 6 (CH 3) 4 0 2, Oxymethylene compounds, characterized by the grouping > C:CH(OH), also give benzene derivatives by hydrolytic condensation between three molecules; thus oxymethylene acetone, or formyl acetone, CH 3 CO.
    0
    0
  • CH :CH (OH), formed by acting on formic ester with acetone in the presence of sodium ethylate, readily yields [1.3.51-triacetylbenzene, C 6 H 3 (CO CH 3) 3; oxymethylene acetic ester or formyl acetic ester or ß-oxyacrylic ester, (HO)CH :CH CO 2 C 2 H 51 formed by condensing acetic ester with formic ester, and also its dimolecular condensation product, coumalic acid, readily yields esters of [1.3.
    0
    0
  • OH COOH,when acetoneoxalic ester, CH 3 CO CH 2 CO CO CO 2 C 2 H 5, is boiled with baryta (Ber., 1889, 22, p. 3271).
    0
    0
  • More important are Kekule's observations that nitrous acid oxidizes pyrocatechol or [I.2]-dioxybenzene, and protocatechuic acid or [3.4]- dioxybenzoic acid to dioxytartaric acid, (C(OH) 2 COOH) 2 (Ann., 1883, 221, p. 230); and 0.
    0
    0
  • Potassium chlorate and hydrochloric acid oxidize phenol, salicylic acid (o-oxybenzoic acid), and gallic acid ([2.3.4] trioxybenzoic acid) to tri chlorpyroracemic acid (isotrichlorglyceric acid), CC13 C(OH)2 C02H, a substance also obtained from trichloracetonitrile, CC1 3 CO CN, by hydrolysis.
    0
    0
  • OH C1t '-C12 (3) C1 3 C co.
    0
    0
  • Thus salicylic acid yields n-pimelic acid, [[Hooc (Ch 2) 5 Cooh]], while o-, m-, and p-cresotinic acids, C 6 H 3 (CH 3)(OH)(000H), yield isomeric methylpimelic acids.
    0
    0
  • C T CI ?OH CI " N O Cl OH _Cl OH C1 2 Nz0 C12 C C Ciz C1 2 Clt Cit (r) (2) (3) (4) CCI /CH2 CU CI C 'CO H CH ?C02H CI C. t 'c% CCI t CH3 (5) (6) 0 C1 /N C1 2 ClZ',C12 NzO C12 (2) CI (3) HO 2 C [[Ccichc1 Cc1 2 Co Cc13 - (6) Ho 2 C Ccichci]] CCl?
    0
    0
  • Kekule (Ann., 1883, 221, p. 230), however, reinvestigated this acid; he showed that it was dibasic and not tribasic; that it gave tartaric acid on reduction; and, finally, that it was dioxytartaric acid, HOOC C(OH) 2 C(OH) 2 COOH.
    0
    0
  • OH(C 2 H 5) 2.
    0
    0
  • Thus a double bond of oxygen, as in the carbonyl group CO, requires a larger volume than a single bond, as in the hydroxyl group - OH, being about 12.2 in the first case and 7.8 in the second.
    0
    0
  • The thermal effect of the " alcohol " group C. OH may be determined by finding the heat of formation of the alcohol and subtracting the thermal effects of the remaining linkages in the molecule.
    0
    0
  • The most important auxochromes are the hydroxyl (- OH) and amino.
    0
    0
  • I OH (I =0)NO 2)=NOiNa.
    0
    0
  • Knorr, by the action of ammonia on aceto-acetic ester, obtained (3-imidobutyric ester, which with nitrous acid yields a-isonitroso-(3-imidobutyric ester, CH 3 C(:NH) C(:N OH) CO 2 C 2 H 5.
    0
    0
  • He also found that diaceto succinic ester reacts with compounds of the type NH 2 R(R = H, CH 3, OH, NHC 6 H 5, &c.) to form pyrrol derivatives CH3 CO CH CO 2 R, C(CH3) :C C02R A NH 2 R -?- - RN(CH 3 CO CH CO 2 R C(CH3) :C C02R By using compounds of the type NH 2 R and acetophenone acetoacetic ester C 6 H 5 CO CH 2.
    0
    0
  • SALICYLIC ACID (ortho-hydroxybenzoic acid), an aromatic acid, C 6 H 4 (OH)(CO 2 H), found in the free state in the buds of Spiraea Ulmaria and, as its methyl ester, in gaultheria oil and in the essential oil of Andromeda Leschenaultii.
    0
    0
  • Methyl Salicylate, C,H 4 (OH) CO 2 CH 31 found in oil of wintergreen, in the oil of Viola tricolor and in the root of varieties of Polygala, is a pleasant-smelling liquid which boils at 222° C. On passing dry ammonia into the boiling ester, it gives salicylamide and dimethylamine.
    0
    0
  • Ethyl salicylate, C 6 H 4 (OH) CO 2 C 2 H 5j is obtained by boiling salicylic acid with alcohol and a little sulphuric acid, or by dropping an alcoholic solution of salicylic acid into 13-naphthalene sulphonic acid at a temperature of 140-150° C. (German Patent 76,574).
    0
    0
  • Phenyl salicylate, C6H4(OH) C 02C6H5, or salol, is obtained by heating salicylic acid, phenol and phosphorus oxychloride to 120-125° C.; by heating salicylic acid to 2 =0° C.; or by heating salicyl metaphosphoric acid and phenol to 140-150° C. (German Patent 85,565).
    0
    0
  • C 4 BUTYL ALCOHOLS H 9 OH.
    0
    0
  • Normal butyl alcohol, CH 3 (CH 2) 2 CH 2 OH, is a colourless liquid, boiling at 116.8°, and formed by reducing normal butyl aldehyde with sodium, or by a peculiar fermentation of glycerin, brought about by a schizomycete.
    0
    0
  • Isobutyl alcohol, (CH 3) 2 CH CH 2 OH, the butyl alcohol of fermentation, is a primary alcohol derived from isobutane.
    0
    0
  • Thomas Moore, who warmly eulogizes Emmet, with whom he was a student at Trinity College, records that one day when he was playing on the piano the melody "Let Erin remember," Emmet started up exclaiming passionately, "Oh, that I were at the head of 20,000 men marching to that air!"
    0
    0
  • The romance of his love affair with Sarah Curran - who afterwards married Robert Henry Sturgeon, an officer distinguished in the Peninsular War - has cast a glamour over the memory of Robert Emmet; and it inspired Thomas Moore's well-known songs, "She is far from the land where her young hero sleeps," and "Oh, breathe not his name"; it is also the subject of Washington Irving's "The Broken Heart."
    0
    0
  • OXIMES, in organic chemistry, compounds containing the grouping > C: N OH, derived from aldehydes and ketones by condensing them with hydroxylamine.
    0
    0
  • Beckmann, Ber., 1886, 1 9, p. 9 8 9; 188 7, 20, p. 2580), yielding as final products an acid-amide or anilide, thus: RC(:N OH)R'-RC(OH) :NR' ---> As regards the constitution of the oximes, two possibilities exist, namely >C: NOH, or > C' ?, and the first of these is presumably correct, since on alkylation and subsequent hydrolysis an alkyl hydroxylamine of the type NH 2 OR is obtained, and consequently it is to be presumed that in the alkylated oxime, the alkyl group is attached to oxygen, and the oxime itself therefore contains the hydroxyl group. It is to be noted that the oximes of aromatic aldehydes and of unsymmetrical aromatic ketones frequently exist in isomeric forms. This isomerism is explained by the HantzschWerner hypothesis (Ber., 1890, 23, p. II) in which the assumption is made that the three valencies of the nitrogen atom do not lie in the same plane.
    0
    0
  • , the former, N OH HO N where the H atom and OH group are contiguous, being known as syn-aldoximes and the latter as the anti-aldoximes.
    0
    0
  • N OH R C R' -SRN: C(OH)R'-->RNH COR' (Rand OH," syn").
    0
    0
  • p. 411), the cycle of reactions probably being as follows: NO 2 [[Nhoh-Hno 2 +Hno]]; HNO-}-RI-CHI+RNO (CH3CH2NO-->CH 3 CH: N OH).
    0
    0
  • The pentose is then obtained from the acetylated compound by successive treatment with ammonia and dilute acids: CH 2 OH ([[Choh) 3 Choh Ch: Noh -)Ch20h (Choh)3 Choh Cn - Ch 2 Oh (Choh) 3 Cho]].
    0
    0
  • -> CH3C6H5CONHC6H51 N OH Syn-phenyltolylketoxime CH3 C6H4 C C6H5 CH3C6H4NH000,H5 HO N A nti-tolylphenylketoxime In the case of the aldoximes, that one which most readily loses the elements of water on dehydration is assumed to contain its hydroxyl radical adjacent to the movable hydrogen atom and is designated the syn-compound.
    0
    0
  • It combines with sulphuric acid to form nitro-sulphonic acid, SO 2 (OH) (N02).
    0
    0
  • Soc., 188 9, 55, p. 760), or when benzsulphohydroxamic acid, C 6 H 5 SO 2 NH OH, is treated in the same manner (0.
    0
    0
  • Thiele, however, regards nitramide as imidonitric acid, HN :NO(OH).
    0
    0
  • Oh the 1st of October 1801 an armistice was signed in London, and the Peace of Amiens followed, on the 27th of March 1802.
    0
    0
  • In aqueous solutions, for instance, a few hydrogen (H) and hydroxyl (OH) ions derived from the water are always present, and will be liberated if the other ions require a higher decomposition voltage and the current be kept so small that hydrogen and hydroxyl ions can be formed fast enough to carry all the current across the junction between solution and electrode.
    0
    0
  • In dilute solution such substances as hydrochloric acid and potash are almost completely dissociated, so that, instead of representing the reaction as HC1+KOH = KC1 d-H20, we must write The ions K and Cl suffer no change, but the hydrogen of the acid and the hydroxyl (OH) of the potash unite to form water, which is only very slightly dissociated.
    0
    0
  • Kiliani in 1885-1887, who showed it to be CH 2 OH (CH OH) 4 CHO.
    0
    0
  • These formulae are supported by many considerations, especially by the selective CH 2 OH CH20H CH OH CH OH C C H O
    0
    0
  • KLi[Al(OH,F)2]Al(S103) 3 Zinnwaldite..
    0
    0
  • (K,Li)3[Al(OH,F)2]FeAl2S15016 Biotite.
    0
    0
  • It is decomposed, on dry distillation, into carbon dioxide and pyromellitic acid, C i oH 6 0 8 i when distilled with lime it gives carbon dioxide and benzene.
    0
    0
  • Water when absolutely pure has no action on lead, but in the presence of air the lead is quickly attacked, with formation of the hydrate, Pb(OH) 2, which is appreciably soluble in water forming an alkaline liquid.
    0
    0
  • The corresponding hydrate, Pb(OH)2, is obtained as a white crystalline precipitate by adding ammonia to a solution of lead nitrate or acetate.
    0
    0
  • Plumbic acid, Pb0(OH) 21 is obtained as a bluish-black, lustrous body of electrolysing an alkaline solution of lead sodium tartrate.
    0
    0
  • A basic chloride, Pb(OH)Cl, was introduced in 1849 by Pattinson as a substitute for white lead.
    0
    0
  • Of greater practical importance is a basic carbonate, substantially 2PbCO 3 Pb(OH) 2, largely used as a white pigment under the name of "white lead."
    0
    0
  • Pb(N03)OH, Pb30(OH)2(N03)2, Pb 3 02(OH)N03, &c., have been described.
    0
    0
  • MANDELIC ACID (Phenylglycollic Acid), C 8 H 8 O 3 or C 6 H 5 CH(OH) COOH, an isomer of the cresotinic and the oxymethylbenzoic acids.
    0
    0
  • CH(OH) �NH.
    0
    0
  • With sodium bisulphite they form the so-called bisulphite compounds R�CH(OH)�SO Na, which are readily resolved into their components by distillation with dilute acids, and are frequently used for the preparation of the pure aldehyde.
    0
    0
  • With hydrocyanic acid aldehydes form the cyanhydrins R�CH(OH)�CN.
    0
    0
  • Hantzsch (Ber., 18 99, 3 2, pp. 577 et seq.) are probably derived from the isomeric iso-nitro compounds R: NO(OH), and thus the nitro derivatives are to be looked upon as pseudo-acids.
    0
    0
  • OH or C i H 5.
    0
    0
  • CH< N OH (see further, A.
    0
    0
  • The following structural formulae are assigned to these compounds: R CAN OH R.CCN(OK) > O R C N02K NO 2 N(:O) NO nitrolic acid; erythro-salt; leuco-salt.
    0
    0
  • RR': C(NO) NO 2 - ERR': C(NH OH) 2 - > RR': C: N 0H+NH20H.
    0
    0
  • 2-dioxy-3-benzoic acid, C 6 113(OH)2000H.
    0
    0
  • Stannous Oxide, SnO, is obtained in the hydrated form Sn20(OH)2 from a solution of stannous chloride by addition of sodium carbonate; it forms a white precipitate, which can be washed with air-free water and dried at 80° C. without much change by oxidation; if it be heated in carbon dioxide the black SnO remains.
    0
    0
  • The crystals are very soluble in cold water, and if the salt is really pure a small proportion of water forms a clear solution; but on adding much water most of the salt is decomposed, with the formation of a precipitate of oxychloride, 2Sn(OH)Cl H20.
    0
    0
  • The structural relations are: nOCH OH / OH 3 f IOCH3 ./11 ??
    0
    0
  • With the possible C 6 H 4 /C (C6H4 OH)2 ?0, CsH /CLCeI14]z0� ?CO ? ?, CO / CO / I.
    0
    0
  • How much of the hydrogen and oxygen are in the hydroxylic (OH) form cannot be absolutely stated, but from the study of the acetates at least three hydroxyl groups may be assumed.
    0
    0
  • It is decomposed readily by water, sodium hydroxide, alcohol and ether: 2SiHF 3 +4H 2 0 = H 4 S10 4 +H 2 SiF 6 -1-211 2; SiHF 3 +3NaOH H 2 O =H4S104+3NaF+H2; 2SiHF 3 +4C 2 H 5 OH =Si(0C 2 H 5) 4 +H 2 SiF 6 +2H 2 i SiHF 3 +3(C 2 H 5) 2 0 =SiH(OC2H5)3+3C2H5F.
    0
    0
  • It is a colourless liquid which boils at 210° C. Water decomposes it with the formation of silico-mesoxalic acid, HOOSi Si(OH) 2 SiOOH.
    0
    0
  • Triethyl silicol, (C2H5),Si OH, is a true alcohol, obtained by condensing zinc ethyl with silicic ester, the resulting substance of composition, (C2H5)3 SiOC2H51 with acetyl chloride yielding a chloro-compound (C2H5)3SiC1, which with aqueous ammonia yields the alcohol.
    0
    0
  • OH) 2, obtained by decomposing silicon hexachloride with icecold water, is an unstable solid which is readily decomposed by the inorganic bases, with evolution of hydrogen and production of a silicate.
    0
    0
  • OSiSi(OH) 2 SiO.
    0
    0
  • OH, formed by the action of moist air on silicon octochloride at o° C., is very unstable, and hot water decomposes it with evolution of hydrogen and formation of silicic acid (L.
    0
    0
  • (2) The organic carbonates are the esters of carbonic acid, H 2 CO 3, and of the unknown ortho-carbonic acid, C(OH) 4.
    0
    0
  • The image of a source of strength p at S outside a sphere of radius a is a source of strength pa/f at H, where 'OS' =f, OH =a2/f, and a line sink reaching from the image H to the centre 0 of line strength - A la; this combination will be found to produce no flow across the surface of the sphere.
    0
    0
  • Taking Ox along OS, the Stokes' function at P for the source S is p cos PSx, and of the source H and line sink OH is p(a/f) cos PHx and - (p/a) (PO - PH); so that = p (cos PSx+f cos PHx PO a PH), (q) and Ili = -p, a constant, over the surface of the sphere, so that there is no flow across.
    0
    0
  • He prepared the cyanhydrins of glucose and fructose, hydrolysed them to the corresponding oxy-acids, from which the hydroxy groups were split out by reduction; it was found that glucose yielded normal heptylic acid and fructose methylbutylacetic acid; hence glucose is an aldehyde alcohol, CH 2 OH (CH OH) 4 CHO, whilst fructose is a ketone alcohol CH 2 OH (CH OH) 3 CO.
    0
    0
  • CH 2 OH.
    0
    0
  • Fischer) CH20H CH20H / CH CH OH (CH OH) 2 -> (CH OH)2 CH-OH CH OH CO CHO -> Lactone -> Hexose.
    0
    0
  • CH 2 OH CH20H CH20H CH20H (CH OH) 3 -> 01 OH) 3 -> (CH OH) 3 --> (CH OH)3 CH OH CH OH CH OH CHO CHO CH:NOH CN Hexose -p Oxime -> Nitrile -> Pentose.
    0
    0
  • hydrogen peroxide and a trace of a ferrous salt: C 4 H 9 O 4 (CH OH) CHO-->C 4 H 9 O 4 (CH OH) C02H->C4H904 CHO Hexose -> Acid -* Pentose.
    0
    0
  • R R R CH OH --o CH OH -> C:N NHPh CHO CH :N NHPh.
    0
    0
  • Glycerin appears to yield, on mild oxidation, an aldehyde, CH20H CH(OH) CHO, and a ketone, CH 2 OH CO CH 2 OH, and these condense as shown in the equation: CH 2 OH CH (OH) CHO + CH 2 OH [[Coch 2 Oh = Ch20h Ch(Oh) Ch(Oh) Ch(Oh) Co.Ch20h+H20]].
    0
    0
  • CH20H CH20H CH OH CH OH (CH OH) 2 -> (CH OH)2 CHO CH-OH CN Pentose -> Cyanhydrin on further oxidation gives a mannonic acid, C 5 H 8 (OH) 5 CO 2 H; this acid readily yields a lactone.
    0
    0
  • Glyceric aldehyde, CH 2 OH CH(OH) CHO, was obtained pure by Wohlon oxidizing acrolein acetal, CH 2 CH(OC 2 H 5) 21 and hydrolysing.
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  • The ketone, dihydroxyacetone, CH 2 OH CO CH 2 OH, was obtained by Piloty by condensing formaldehyde with nitromethane, reducing to a hydroxylamino compound, which is oxidized to the oxime of dihydroxyacetone; the ketone is liberated by oxidation with bromine water: 3H CHO + CH 3 NO 2 -- (CH 2 OH) 3 C NO 2 - (CH 2 OH) 3 C NH OH -- (CH 2 OH) 2 C: NOH - > (CH20H)2CO.
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  • Arabinose being convertible into /-glucose and xylose into l-gulose, the alternative formulae to be considered are CH 2 (OH) - - - +COH CH 2 (OH) + + - COH.
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  • If the asymmetric system adjoining the COH group, which is that introduced in synthesizing the hexose from the pentose, be eliminated, the formulae at disposal for the two pentoses are CH 2 (OH) - - - COH CH 2 (OH)+-- COH.
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  • When such compounds are converted into corresponding dibasic acids, CO 2 H.[CH(OH)) 3.00 2 H, the number of asymmetric carbon atoms becomes reduced from three to two, as the central carbon atom is then no longer associated with four, but with only three different radicles.
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  • As a matter of fact, only arabinose gives an active product on oxidation; it is therefore to be supposed that arabinose is the - - - compound, and consequently CH 2 (OH) - - - + COH = /-glucose CH 2 (OH) + - - - COH = l-gulose.
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  • It follows from the manner in which l-idose is produced that its configuration is CH 2 (OH) + - - +COH.
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  • It can be shown that d-galactose is CH 2 (OH) + - + - COH, and hence d-talose is CH 2 (OH) + - + + COH.
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  • as containing the group CH(OH) CHO.
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  • Other zinc minerals are willemite, Zn 2 SiO 4, hydrozincite or zinc bloom, ZnCO 3.2Zn(OH)2, zincite or red zinc ore, ZnO, and franklinite, 3(Fe,Zn)0 (Fe,Mn) 2 0 3 .
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  • Boiling water attacks it appreciably, but slightly, with evolution of hydrogen and formation of the hydroxide, Zn(OH) 2.
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  • Zinc hydroxide, Zn (OH) 2, is prepared as a gelatinous precipitate by adding a solution of any zinc salt to caustic potash.
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  • Zinc carbonate, ZnCO 3, occurs in nature as the mineral calamine (q.v.), but has never been prepared artificially, basic carbonates, ZnCO 3 .xZn(OH) 2, where x is variable, being obtained by precipitating a solution of the sulphate or chloride with sodium carbonate.
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  • 3 (P04)2.4H20, and tarbuttite, Zn 3 (P04)2.Zn(OH)2, both found in Rhodesia.
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  • OH(2), occurs as sulphate in the urine of the horse.
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  • OH(3), is formed when thymol (paraisopropyl-meta-cresol) is heated with phosphorus pentoxide.
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  • OH(4), occurs as sulphate in the urine of the horse.
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  • unites with C(OH) >C6114 C 6 11 4 /C6114 (y) (anthranol) is a reduction product of anthraquinone.
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  • The solution, if boiled, deposits its titanic oxide as a hydrate called metatitanic acid, TiO(OH) 21 because it differs in its properties from orthotitanic acid, Ti(OH) 4, obtained by decomposing a solution of the chloride in cold water with alkalis.
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  • According to the amount of water used, TiC1 3 OH, TiC1 2 (OH) 21 TiCI(OH) 3 or titanic acid is formed.
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  • OH NH(CH 3) 2.
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  • The aqueous solution of the amines is now shaken up with diethyl oxalate, when the primary amine forms a crystalline dialkyl oxamide and the secondary amine an insoluble liquid, which is an ethyl dialkyl oxamate, the tertiary amine not reacting: (C02C2H5)2+ 2NH 2 R = (CO�NHR) 2 -{- 2C 2 H S OH; (CO 2 C 2 H 5) 2 -}- NHR 2 = C 2 H S O 2 C�Conr 2 -1-C 2 H S Oh.
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  • The amorphous form readily slakes with water, and the aqueous solution yields a crystalline hydrated hydroxide approximating in composition to Sr(OH) 2.8H 2 O or Sr(OH) 2.9H 2 O, which on standing in vacuo loses some of its water of crystallization, leaving the monohydrated hydroxide, Sr(OH) 2 H 2 O.
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  • OH, termed the carboxyl group, in which the hydrogen atom is replaceable by metals with the formation of salts, and by alkyl radicals with the formation of esters.
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  • Thus primary alcohols and aldehydes, both of the aliphatic and aromatic series, readily yield on oxidation acids containing the same number of carbon atoms. These reactions may be shown thus: - � R�CH 2 OH -> R.
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  • CH3 OH
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  • When a concentrated solution of auric chloride is treated with caustic potash, a brown precipitate of auric hydrate, Au(OH) 3, is obtained, which, on heating, loses water to form auryl hydrate, AuO(OH), and auric oxide, Au 2 0 3.
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  • 3H20, but it may be an ammine of the formula [Au(NH 3) 2 (OH) 2 ]OH.
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  • I a the basic tellurate montanite, Bi 2 (OH) 4 TeO 4; the silicates eulytite and agricolite, B14(S104) 3; and the uranyl arsenate walpurgite, Bi(U02)3(OH)24(As04)4.
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  • The hydrate, Bi(OH) 3 i is obtained as a white powder by adding potash to a solution of a bismuth salt.
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  • Another basic carbonate, 3(BiO) 2 CO 3.2Bi(OH)3.3H20, constitutes the mineral bismutite.
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  • The action of water on this solution produces a crystalline precipitate of basic nitrate, probably Bi(OH)2N03, though it varies with the amount of water employed.
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  • Water decomposes it, giving a basic salt, Bi 2 (SO 4)(OH) i which on heating gives (BiO) 2 SO 4.
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  • Klein's solution, an aqueous solution of cadmium borotungstate, 2Cd(OH)2-B203.9W03.16H20, introduced by D.
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  • Caesium hydroxide, Cs(OH) 2, obtained by the decomposition of the sulphate with baryta water,is a greyish-white deliquescent solid,which melts at a red heat and absorbs carbon dioxide rapidly.
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  • The steady progress of the heretical movement in spite of all opposition was a cause of deep sorrow to Polycarp, so that in the last years of his life the words were constantly on his lips, "Oh good God, to what times hast thou spared me, that I must suffer such things!"
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  • C (OH): C 6 H 4; and with hydriodic acid at i so C. or on distillation with zinc dust, the hydrocarbon anthracene, C 14 H 10.
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  • METHYL ALCOHOL (CH 2 OH), the simplest aliphatic alcohol; an impure form is known in commerce as wood-spirit, being produced in the destructive distillation of wood.
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  • OH, and with barium oxide BaO.
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