C-1 sentence example

c-1
  • The potential gradient is in all cases lower in summer than winter, and thus the reduction in c 1 in summer would appear even larger than in Table V.
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  • Foreign c I Foreign C 1
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  • After a very short interval of time, the length of which depends on the inductive retardation of the cable, the condensers corresponding to C 1 and C3 at the other end begin to be charged from the cable, and since the charge of C3 passes through the receiving instrument I or G the signal is recorded.
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  • 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.
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  • 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.
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  • 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?
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  • We consider the quantic to have any n number of equivalent representations a- b n -c n So that a 1 -k a 2 = b l -k b 2 - c 1 -k c 2 = ...
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  • Tetranitromethane, C(N02)4, obtained by adding nitroform to a hot mixture of nitric and sulphuric acids, is a crystalline solid which melts at 13° C. Chlorpicrin, CC1 3 NO 2, is a liquid of suffocating odour obtained by the action of nitric acid and chloride of lime on many organic compounds.
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  • Bassett, Ann., 186 4, 1 3 2, P. 54), CC1 3 NO 2 +4C,H 5 ONa= C (0C 2 H 5) 4 +NaNO 2 -}-3NaC1.
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  • When the liquid is bounded externally by the fixed ellipsoid A = A I, a slight extension will give the velocity function 4 of the liquid in the interspace as the ellipsoid A=o is passing with velocity U through the confocal position; 4 must now take the formx(1'+N), and will satisfy the conditions in the shape CM abcdX ¢ = Ux - Ux a b x 2+X)P Bo+CoB I - C 1 (A 1 abcdX, I a1b1cl - J o (a2+ A)P and any'confocal ellipsoid defined by A, internal or external to A=A 1, may be supposed to swim with the liquid for an instant, without distortion or rotation, with velocity along Ox BA+CA-B 1 -C1 W'.
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  • Consider, for example, a submarine boat under water; the inertia is different for axial and broadside motion, and may be represented by (1) c 1 =W+W'a, c2=W+W'/3' where a, R are numerical factors depending on the external shape; and if the C.G is moving with velocity V at an angle 4) with the axis, so that the axial and broadside component of velocity is u = V cos 0, v =V sin 4), the total momentum F of the medium, represented by the vector OF at an angle 0 with the axis, will have components, expressed in sec. Ib, F cos 0 =c 1 - = (W +W'a) V cos 43, F sin 0 = c 2.11 = (W +W'/3) V sin 4) .
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  • (9) (io) (II) F 2 (X 2 +Y 2) = y12+y22 +y32G2, c 2 - c 1 +a u2 h W c2 g = (?
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  • The effective angular inertia of the body in the medium is now required; denote it by C 1 about the axis of the figure, and by C2 about a diameter of the mean section.
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  • A rotation about the axis of a figure of revolution does not set the medium in motion, so that C 1 is.
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  • the moment of inertia of the body about the axis, denoted by But if is the moment of inertia of the body about a mean diameter, and w the angular velocity about it generated by an impluse couple M, and M' is the couple required to set the surrounding medium in motion, supposed of effective radius of gyration k', If the shot is spinning about its axis with angular velocity p, and is precessing steadily at a rate about a line parallel to the resultant momentum F at an angle 0, the velocity of the vector of angular momentum, as in the case of a top, is C i pµ sin 0- C2µ 2 sin 0 cos 0; (4) and equating this to the impressed couple (multiplied by g), that is, to gN = (c 1 -c 2)c2u 2 tan 0, (5) and dividing out sin 0, which equated to zero would imply perfect centring, we obtain C21 2 cos 0- (c 2 -c 1)c2u 2 sec 0 =o.
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  • In the extreme case when e=1, the prolate ellipsoid becomes a long thin rod, and then the capacity is given by C 1 = a/log e 2a/b (io), which is identical with the formula (2) already obtained.
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  • If the trapezette, as seen from above, is everywhere convex or everywhere concave, the true area lies between C 1 and T1.
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  • ' 1(9 C 1 - C 3) -` i - C1 + -s(C 1 - C3).
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  • The fact that C 1 does not give the true area is due to the fact that in passing from one extremity of the top of any strip to the other extremity the tangent to the trapezette E, _- changes its direction.
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  • x=xo, and an analogous formula (which may be obtained by substituting 2h and C, for h and C 1 in the above and then expressing T 1 as 2C -CO) A =J xo udx=T1+ [4h2u'_+ 15487$5 h8uvii ?
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  • In order to find the corrections in respect of the terms shown in square brackets in the formulae of § 75, certain ordinates other than those used for C 1 or T I are sometimes found specially.
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  • If we use c 1 to represent the chord of the whole arc, c 2 the chord of half the arc, and c 4 the chord of one quarter of the arc, then corresponding to (i) and (iii) of § 70 or § 79 we have a (8c 2 - c i) and4 5 (256c 4 - 40c2+ci) as approximations to the length of the arc. The first of these is Huygens's rule.
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  • If, for the single toothed wheel, be substituted a set of four with a common axis, in which the teeth are in the ratios 4: 5: 6: 8, and if the card be rapidly passed along their edges, we shall hear distinctly produced the fundamental chord C, E, G, C 1 and shall thus satisfy ourselves that the intervals C, E; C, G and C, C 1 are, 2 and 2 respectively.
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  • Exact formulae are: - Area = 2a 2 (0 - sin 0)=1a 2 0 - 4c2 cot zB =Za 2 -2 c?1 (a 2 -4c 2).
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  • Take AB equal to one-fourth of the given line; on AB describe a square ABCD; join AC; in AC produced find, by a known process, a point C 1 such that, when C 1 B 1 is drawn perpendicular to AB produced and C 1 D 1 perpendicular to BC produced, the rectangle BC,.
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  • In This Case, X=18 39, () W (149) W = 459, C = 18, C 16=2, 4 C 1 And (46) W =O.
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  • A 2.6 naphthoquinone results on oxidizing 2.6 dihydroxynaphthalene with lead Or Hydroxynaphthalenes, C 1 oH 7 OH, the naphthalene homologues of the phenols.
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  • When heated with hydrazine hydrate at 150° C. it gives a-naphthyl hydrazine, C 1 oH 7 NH NH 2 Hoffmann, Ber., 1898, 31, p. 2909).
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  • The most important is Nevile and Winther's acid, C 1 aHe(OH)(SO 3 H)(I.
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  • 0-Naphthol, C 1 oH 7 OH, prepared by fusing sodium 0-naphthalene sulphonate with caustic soda, crystallizes in plates which melt at 122° C. With ferric chloride it gives a green colouration, and after a time a white flocculent precipitate of a dinaphthol.
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  • a-Naphthoic acid, C 1 oH 7 CO 2 H, is formed by hydrolysis of the nitrile, obtained by distilling potassiuma-naphthalene sulphonate with potassium cyanide (V.
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  • It forms needles which melt at 160° C. (3-Naphthoic acid, obtained b y boiling 0-methylnaphthalene with dilute nitric acid, or by hydrolysis of its nitrile (formed when formyl-0-naphthalide is heated with zinc dust), crystallizes from alcohol in needles which Nitrosonaplithols or naphthoquinone-oxames, C 1 oH 6 (OH)(NO) or melt at 184° C. C 1 oH 6 (: NOH): 0.
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  • Now taking the isomers H 3 C CC1 3 (M„ = 108) and C1H 2 C CHC1 2 (M„ = we see the negative chlorine atoms heaped up in the left hand formula, but distributed in the second; the former therefore may be presumed to occupy a larger space, the molecular volume, that is, the volume in cubic centimetres occupied by the molecular weight in grams, actually being 108 in the former, and 103 in the latter case (compare Chemistry: Physical).
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  • If A 1, C 1 are the disks, so that the distance between them is less than irr, the curve must be produced beyond the disks before it is at its mean distance from the axis.
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  • Campholic acid, C 1 oH 18 0 2, is tetramethyl-1.2.2.3-cyclo-pentane acid-3.
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  • Euterpene (trimethyl-i 4.4-cyclo-heptadiene 1.5), C 1 oH 1 s is prepared from dihydroeucarveol.
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  • Just as e before a syllable in ivhich an i occurs is changed into I, so in the same circumstances o becomes u (full, folium;vuil, volio forvoleo)andalsowhentheaccented vowel precedes a group of consonants like ci, p1, and the like (ull, o c 1 u s; escull, Sd 0 p I u s).
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  • cl, ij gives y: veyu (*v e c 1 u s), espeyu (s p e cl u m), conseyu (c 0 n s iii u m); and after an i this y is hardly perceptible, to judge by the forms flu (f i Ii u m), escoidos (Cast.
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  • The alteration that takes place in the regular diurnal inequality throughout the year is best seen by analysing it into a Fourier series of the type c 1 sin (t+ a l) +c2 sin (2t+ a 2)+c 3 sin (3t+a3)+c4 sin (4t+a 4)+..
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  • When one of the levers of K is depressed, the condenser C 1 and the cable, and the condenser C2 and the artificial cable, are simultaneously charged in series; but, if the capacity of C 1 bears the same proportion to the capacity of the cable as the capacity of C2 bears to the capacity of the artificial cable, and if the other adjustments are properly made, no charge will be communicated to C3.
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  • HO 2 C CCI:CCI CO CC1 3 ' - > H02C CC1:cC1 c02H+CHe13' (to) (xi) Hydroquinone (1.4 or para-dioxybenzene) (1) gives with chlorine, first, a tetrachlorquinone (2), and then hexachlor-p-diketo-R-hexene (3), which alcoholic potash converts into perchloracroylacrylic acid (4).
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  • Put M 1 For M, N I For N, And Multiply Through By (Ab); Then { (F, C6) } = (Ab) A X 2A Y B X 1 M N I 2 (Xy), ?) 2, = (A B)Ax 1B X 2B Y L I Multiply By Cp 1 And For Y L, Y2 Write C 2, C1; Then The Right Hand Side Becomes (Ab)(Bc)Am Lbn 2Cp 1 M I C P (F?) 2 M { N2 X, Of Which The First Term, Writing C P =, ,T, Is Mn 2 A B (Ab)(Bc)Axcx 1 M 2 N 2 P 2 2222 2 2 _2 A X B X C (Bc) A C Bx M N 2 2 2 M2°N 2 N 2 M 2 2 A X (Bc) B C P C P (Ab) A B B(Ac) Ax Cp 2 = 2 (04) 2 1 (F,0) 2.4 (F,Y') 2 �?; And, If (F,4)) 1 = Km " 2, (F??) 1 1 M N S X X X Af A _Af A Ax, Ax Ax Ax1 Observing That And This, On Writing C 2, C 1 For Y 11 Y 21 Becomes (Kc) K X 'T 3C X 1= (F,0 1 ', G 1; �'�1(F,O) 1 M 1=1 M 2 0`,4)) 2 0, T (Fm 2.4 (0,0 2 .F ' And Thence It Appears That The First Transvectant Of (F, (P) 1 Over 4) Is Always Expressible By Means Of Forms Of Lower Degree In The Coefficients Wherever Each Of The Forms F, 0, 4, Is Of Higher Degree Than The First In X 1, X2.
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  • Tetranitromethane, C(N02)4, obtained by adding nitroform to a hot mixture of nitric and sulphuric acids, is a crystalline solid which melts at 13° C. Chlorpicrin, CC1 3 NO 2, is a liquid of suffocating odour obtained by the action of nitric acid and chloride of lime on many organic compounds.
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  • If R I and R2 are the arms' resistances and C 1 and C2 the condenser capacities, then when the bridge is balanced we have R l: R2= C l: C2.
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  • To illustrate the method, suppose that we use the chordal area C1, and that the trapezette is in fact parabolic. The difference between C 1 and the true area is made up of a series of areas bounded by chords and arcs; this difference becoming less as we subdivide the figure into a greater number of strips.
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  • 'NAPHTHALENE, C 1 oH 8, a hydrocarbon discovered in the "carbolic" and "heavy oil" fractions of the coal-tar distillate '(see Coal-Tar) in 1819 by A.
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  • When heated with hydrazine hydrate at 150° C. it gives a-naphthyl hydrazine, C 1 oH 7 NH NH 2 Hoffmann, Ber., 1898, 31, p. 2909).
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  • 0-Naphthol, C 1 oH 7 OH, prepared by fusing sodium 0-naphthalene sulphonate with caustic soda, crystallizes in plates which melt at 122° C. With ferric chloride it gives a green colouration, and after a time a white flocculent precipitate of a dinaphthol.
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  • It forms needles which melt at 160° C. (3-Naphthoic acid, obtained b y boiling 0-methylnaphthalene with dilute nitric acid, or by hydrolysis of its nitrile (formed when formyl-0-naphthalide is heated with zinc dust), crystallizes from alcohol in needles which Nitrosonaplithols or naphthoquinone-oxames, C 1 oH 6 (OH)(NO) or melt at 184° C. C 1 oH 6 (: NOH): 0.
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  • Within the word the same group and other groups also in which the second consonant is an 1 produce I mouillOe (Written ih, just as n mouillOe is written nh, as in Provenal): oveiha (0 V i c I a), veiho (*v e c 1 u s); and sometimes ch: fec/jo (f a cl urn), ancho (am plum).
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