Organic Chemistry volume 2
Organic Chemistry volume 2
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In our eReader you can find the full English version of the book. Read Organic Chemistry volume 2 Online - link to read the book on full screen. Our eReader also allows you to upload and read Pdf, Txt, ePub and fb2 books. In the Mini eReder on the page below you can quickly view all pages of the book - Read Book Organic Chemistry volume 2
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1-095 at 20, and boils at 239. It has a peculiar charac- teristic smell, and is sparingly soluble in water, but it dissolves freely in dilute acids, forming crystalline salts, such as the hydrochloride, C 9 H 7 N, HC1, the sulphate, (C 9 H 7 N) 2, H 2 S0 4, &c. It also forms double salts, of which the platinochloride, (C 9 H 7 N) 2, H 2 PtCl 6 + 2H 2 0, and the bichromate, (C 9 H 7 N) 2, H 2 2 7, may be mentioned ; the latter, prepared by adding potassium bichromate to a solution of quinoline h...ydrochloride, crystal- lises from water, in which it is only sparingly soluble, in glistening yellow needles, melting at 164-167.
Quinoline is a tertiary base (compare p. 484), and com- bines, with methyl iodide, to form the additive product, quinoline methiodide, C 9 H 7 N, CH 3 I.
Constitution. As the relation between pyridine, C 5 H 5 N, and quinoline, C 9 H 7 N, on the one hand, is much the same as that between benzene, C 6 H 6, and naphthalene, C 10 H 8, on the other, both as regards chemical behaviour and molecular composition (the difference being C 4 H 2 in both cases), it might be assumed that quinoline is derived from pyridine, just as naphthalene is derived from benzene ; consequently the constitution of quinoline might be expressed by one of the following formulas : CH CH CH CH ^^\CH CH N CH CH I.
What to read after Organic Chemistry volume 2?
You can find similar books in the "Read Also" column, or choose other free books by W H William Henry Perkin to read onlineMoreLess
To quickly assess the difficulty of the text, read a short excerpt:
1-095 at 20, and boils at 239. It has a peculiar charac- teristic smell, and is sparingly soluble in water, but it dissolves freely in dilute acids, forming crystalline salts, such as the hydrochloride, C 9 H 7 N, HC1, the sulphate, (C 9 H 7 N) 2, H 2 S0 4, &c. It also forms double salts, of which the platinochloride, (C 9 H 7 N) 2, H 2 PtCl 6 + 2H 2 0, and the bichromate, (C 9 H 7 N) 2, H 2 2 7, may be mentioned ; the latter, prepared by adding potassium bichromate to a solution of quinoline h...ydrochloride, crystal- lises from water, in which it is only sparingly soluble, in glistening yellow needles, melting at 164-167.
Quinoline is a tertiary base (compare p. 484), and com- bines, with methyl iodide, to form the additive product, quinoline methiodide, C 9 H 7 N, CH 3 I.
Constitution. As the relation between pyridine, C 5 H 5 N, and quinoline, C 9 H 7 N, on the one hand, is much the same as that between benzene, C 6 H 6, and naphthalene, C 10 H 8, on the other, both as regards chemical behaviour and molecular composition (the difference being C 4 H 2 in both cases), it might be assumed that quinoline is derived from pyridine, just as naphthalene is derived from benzene ; consequently the constitution of quinoline might be expressed by one of the following formulas : CH CH CH CH ^^\CH CH N CH CH I.
What to read after Organic Chemistry volume 2?
You can find similar books in the "Read Also" column, or choose other free books by W H William Henry Perkin to read onlineMoreLess
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