Author Question: Identify X and Y in the following reaction. a. X is 4-methylpentane-3,4-diol, and Y is ... (Read 78 times)

kshipps · **on:** Aug 23, 2018

Identify X and Y in the following reaction.

a.
X is 4-methylpentane-3,4-diol, and Y is HIO₄.

b.
X is 3-methylpentane-2,3-diol, and Y is HIO₃.

c.
X is 2-methylpentane-2,3-diol, and Y is HIO₄.

d.
X is 2-methylpentane-2,3-diol, and Y is HIO₃.

Question 2

Identify X and Y in the following reaction.

a.
X is 3-methylbutan-1-al, and Y is H₂CrO₄/H₂O/acetone.

b.
X is 2-methylbutan-1-ol, and Y is H₂CrO₄/H₂O/acetone.

c.
X is 3-methylbutan-1-ol, and Y is H₂CrO₄/H₂O/acetone.

d.
X is 2-methylbutan-1-al, and Y is H₂CrO₄/H₂O/acetone.

Question 3

The oxidation states of iodine in periodic acid and iodic acid are _____ and _____, respectively.

a.
7; 5

b.
5; 7

c.
7; 7

d.
6; 5

Question 4

Why cant tertiary alcohols be oxidized to ketones or aldehydes?

ndhahbi · **Reply #1 on:** Aug 23, 2018

Answer to Question 1

c

Answer to Question 2

b

Answer to Question 3

a

Answer to Question 4

The prerequisite for the oxidation of alcohol to a ketone or an aldehyde is the presence of a free hydrogen atom on the carbon-bearing hydroxyl group. In tertiary alcohols, the carbon bearing the hydroxyl group is bonded with three more carbon atoms but not to the hydrogen atoms. Hence, tertiary alcohols are resistant to oxidation as they cannot form any additional carbonoxygen bond.