Show how you would accomplish the following syntheses efficiently (you may use any necessary reagents).
(a) trans-1-bromobut-2-ene → trans-pent-3-enoic acid (two ways)
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Show how you would accomplish the following syntheses efficiently (you may use any necessary reagents).
(a) trans-1-bromobut-2-ene → trans-pent-3-enoic acid (two ways)
Predict the products (if any) of the following acid–base reactions.
(d) α-bromopropionic acid + sodium propionate
(e) benzoic acid + sodium phenoxide
Show how you would accomplish the following syntheses efficiently (you may use any necessary reagents).
(b) hex-3-ene → propanoic acid
Arrange each group of compounds in order of increasing acidity.
(a) phenol, ethanol, acetic acid
(b) p-toluenesulfonic acid, acetic acid, chloroacetic acid
(c) benzoic acid, o-nitrobenzoic acid, m-nitrobenzoic acid
(d) butyric acid, α-bromobutyric acid, β-bromobutyric acid
(e)
Given the structure of ascorbic acid (vitamin C):
(c) Predict which proton in ascorbic acid is the most acidic.
(d) Draw the form of ascorbic acid that is present in the body (aqueous solution, pH = 7.4)
Rank the following isomers in order of increasing boiling point, and explain the reasons for your order of ranking.