N-c sentence example

n-c
  • Thurnlach, Annalen, 1882, 213, p. 369) th: - Z us n(C H) H20 CH �CHO - > CH3�CHCH3�CH
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  • Then, since nr rl is also a rational integral function of n of degree r, we can find a coefficient c r, not containing n, and such as to make N-c r nr ri contain no power of n higher than n r - 1.
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  • Busch, Ber., 1899, 32, p. 2960): N C(SH):N C 6 H 5 /N C:NC6H5 C. 2 S 7Hs " H s d-H N NH C,H 7 C7 "N N C,H7 C. Harries (Ber., 1895, 28, p. 1223) has also shown that as-phenylhydrazino-acetic esters, when heated with formamide and substituted formamides under pressure, yield dihydrotriazines: CO 2 R CO-NR'-CH H2 N(C6H5)NH2 +R'NH CHO --> CH 2 N(C 6 H 5) IV The phen-a-triazines are yellow-coloured crystalline compounds of a somewhat basic character.
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  • CH 3C2H5 CH CO N C CH :C - CH2 - CH CH2/0
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  • soc. chim., 18 94 (3) 11, p. 1129) obtained anilino-derivatives of the paraquinones by the action of an aqueous solution of potassium chromate on an acetic acid solution of para-aminodimethylaniline and phenol: C 6 H 5 OH+H 2 N C 6 H 4 N (CH 3) 2 - *O:C 6 H 4 :N C 6 H 4 N(CH 3) 2; these compounds yield the quinone when heated with mineral acids.
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  • AZOXIMES (furo [a.b.] diazoles), a class of organic compounds which contain the ring system N C = CH O.
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  • Methyl orange (helianthin, gold orange, Mandarin orange), (CH 3) 2 N C 6 H 4 N 2 C 6 H 4 SO 3 Na, is the sodium salt of paradimethylaminobenzene-azo-benzene sulphonic acid.
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  • Diazoamino benzene, C 6 H 5 N: N NHC 6 H 5, was first obtained by P. Griess (Ann., 1862, 121, p. 258).
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  • With aniline it forms benzylidine aniline C 6 H 5 CH: N C 6 H 5, and with acetone, benzal acetone C 6 H 5 CH: CH CO CH 3.
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  • HO C(C 6 H 4 NH 2) 3 HC1=H 2 0+(H 2 N C 6 H 4) 2 C: C 6 H 4: NH2C1.
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  • Pararosaniline was reduced to the corresponding leuco compound (paraleucaniline), from which by diazotization and boiling with alcohol, the parent hydrocarbon was obtained (H 2 N C 5 H 4) 2 C:C 6 H 4 :NH 2 Cl - HC(C6H4NH2 HCl)3 - >HC(C6H4N2C13) Pararosaniline hydrochloride.
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  • They combine with hydrocyanic acid to form nitriles, which on hydrolysis furnish hydroxyacids, (CH3)2C0 -> (CH 3) 2 C OH CN - (CH3)2 C OH C02H; with phenylhydrazine they yield hydrazones; with hydrazine they yield in addition ketazines RR' C:N N:C RR' (T.
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  • C 6 H,N 2 NHC 6 H 6+2HC1+H NO 2 =2C6H5N2C1+2H20.
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  • Diazoaminobenzene, C 6 H 5 N 2 NHC 6 H 61 crystallizes in golden yellow laminae, which melt at 96°C. and explode at a slightly higher temperature.
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  • The presence of the phenanthrene nucleus and the chain system CH 3 N C C follows from the fact that these alkaloids, by appropriate treatment, yield a substituted phenanthrene and also dimethylaminoethanol (CH3)2N CH2 CH20H.
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  • CO HO C:N-C OH M.
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  • Let OZ be an axis, as nearly vertical as it can easily be set, round which () N C A B the entire instrument may revolve through 180°.
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  • Bet ore the tonic the same change between a and e constantly takes place; one finds in manuscripts enar, emor for anar, amor (the same extends even to the case of the tonic syllable, ten and sent from t a n t u in and 1 a n c t u m being far from rare), and, on the other hand, antre, arrar, for entre, errar.
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  • Thurnlach, Annalen, 1882, 213, p. 369) th: - Z us n(C H) H20 CH �CHO - > CH3�CHCH3�CH
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  • Bamberger, Ber., 1893, 26, p. 2786): CsH5N :N N :N jC COC6H5 - C6H5NH2+C6H4K C 6 H5 NH N N:C 0006H5; by the reduction of symmetrical acyl-ortho-nitrophenyl hydrazines (e.g.
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  • 8 nec sustinebo in his quae inique exercent, that is n tit: in 9 vindicans vindicabo: in 22 non parcet dextera mea super peccatores = ckio-erac. ...
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  • Diazoaminobenzene, C 6 H 5 N 2 NHC 6 H 61 crystallizes in golden yellow laminae, which melt at 96°C. and explode at a slightly higher temperature.
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  • No S yn r am t n c k r Yatton O Chew W00]SPPIN4 AMa na Br`adford Melksha4zt °WestOn super O / Wilc er Mare Devrzes KP A See d Willow ?.
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  • Let OZ be an axis, as nearly vertical as it can easily be set, round which () N C A B the entire instrument may revolve through 180°.
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  • Source comments: S C R U N C H Figaro routine to scrunch a spectrum or set of spectra.
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