The Identification of Organic Compounds
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137.
Reduction with sodium amalgam produces benzoic acid.
ra-Chlorobenzoie Acid, M. P. 153.
p-Chlorobenzoie Acid, M. P. 236.
o-Bromobenzoie Acid, C 6 H 4 M - m-Nitrobenzoic Acid, M. P. 141. P-Nitrobenzoic Acid, M. P. 238.
These acids can be reduced to the corresponding amino-acids by tin and hydochloric acid.
o-Nitrocinnamic Acid, C fl : CH . COOHj M. P. 237-240.
m-Nitroeinnamie Acid, light yellow needles. M. P. 197.
p-Nitrocinnamic Acid, M. P. 286.
Oxidation with alkaline potassium permangana...te solution converts these acids into the corresponding nitrobenzaldehyde and nitrobenzoic acid.
D. AMINO ACIDS.
Aminoacetic Acid (glycine), CH 2 NH 2 -COOH, M. P. 232, with decomposition, is converted by nitrous acid into glycollic acid.
What to read after The Identification of Organic Compounds?
You can find similar books in the "Read Also" column, or choose other free books by George Ballingall Neave to read onlineMoreLess
To quickly assess the difficulty of the text, read a short excerpt:
137.
Reduction with sodium amalgam produces benzoic acid.
ra-Chlorobenzoie Acid, M. P. 153.
p-Chlorobenzoie Acid, M. P. 236.
o-Bromobenzoie Acid, C 6 H 4 M - m-Nitrobenzoic Acid, M. P. 141. P-Nitrobenzoic Acid, M. P. 238.
These acids can be reduced to the corresponding amino-acids by tin and hydochloric acid.
o-Nitrocinnamic Acid, C fl : CH . COOHj M. P. 237-240.
m-Nitroeinnamie Acid, light yellow needles. M. P. 197.
p-Nitrocinnamic Acid, M. P. 286.
Oxidation with alkaline potassium permangana...te solution converts these acids into the corresponding nitrobenzaldehyde and nitrobenzoic acid.
D. AMINO ACIDS.
Aminoacetic Acid (glycine), CH 2 NH 2 -COOH, M. P. 232, with decomposition, is converted by nitrous acid into glycollic acid.
What to read after The Identification of Organic Compounds?
You can find similar books in the "Read Also" column, or choose other free books by George Ballingall Neave to read onlineMoreLess
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