C-1 sentence example

c-1
  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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