Chapter 16: 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 16: 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 freeExcess ascorbic acid is excreted in the urine, the \(\mathrm{pH}\) of which is normally in the range 4.8-8.4. What form of ascorbic acid would you expect to be present in urine of \(\mathrm{pH} 8.4\) free ascorbic acid or ascorbate anion? Explain.
Show how to prepare pentanoic acid from each compound. (a) 1-Pentanol (b) Pentanal (c) 1-Pentene (d) 1-Butanol (e) 1-Bromopropane (f) 1-Hexene
The normal \(\mathrm{pH}\) range for blood plasma is 7.35-7.45. Under these conditions, would you expect the carboxyl group of lactic acid ( \(\mathrm{p} K_{\mathrm{a}} 3.08\) ) to exist primarily as a carboxyl group or as a carboxylic anion? Explain.
Using your roadmaps as a guide, show how to convert 5 -chloro-2-pentanone and carbon dioxide into racemic tetrahydro-6-methyl-2-pyranone. You must use 5-chloro2-pentanone and carbon dioxide as the source of all carbon atoms in the racemic target molecule. Show all reagents and all molecules synthesized along the way.
Show how cyclohexanecarboxylic acid could be synthesized from cyclohexane in good yield.
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