Chapter 17: Problem 10
Draw a structural formula for each salt. (a) Sodium benzoate (b) Lithium acetate (c) Ammonium acetate (d) Disodium adipate (e) Sodium salicylate (f) Calcium butanoate
Chapter 17: Problem 10
Draw a structural formula for each salt. (a) Sodium benzoate (b) Lithium acetate (c) Ammonium acetate (d) Disodium adipate (e) Sodium salicylate (f) Calcium butanoate
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Get started for freeWrite the IUPAC name of each compound, showing stereochemistry where relevant.
(a)
Using your roadmaps as a guide, show how to convert cyclohexane into adipoyl dichloride. Show all reagents and all molecules synthesized along the way.
When heated, carboxylic salts in which there is a good leaving group on the
carbon beta to the carboxylate group undergo decarboxylation/elimination to
give an alkene.
(a)
Select the stronger acid in each set. (a) Phenol \(\left(\mathrm{p} K_{\mathrm{a}} 9.95\right)\) and benzoic acid \(\left(\mathrm{p} K_{\mathrm{a}} 4.19\right)\) (b) Lactic acid \(\left(K_{\mathrm{a}} 8.4 \times 10^{-4}\right)\) and ascorbic acid \(\left(K_{\mathrm{a}} 7.9 \times 10^{-5}\right)\)
Draw a structural formula for each compound. (a) Phenylacetic acid (b) 4-Aminobutanoic acid (c) 3-Chloro-4-phenylbutanoic acid (d) Propenoic acid (acrylic acid) (e) (Z)-3-Hexenedioic acid (f) 2-Pentynoic acid (g) Potassium phenylacetate (h) Sodium oxalate (i) 2-Oxocyclohexanecarboxylic acid (j) 2,2-Dimethylpropanoic acid
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