Predict the reagents or reactant(s) necessary to complete the following syntheses.
(b)

Predict the product(s) that would result when the alkenes are allowed to react under the following conditions: (viii) 1. O₃ 2. CH₃SCH₃

(k)

Predict the product(s) that would result when the alkenes are allowed to react under the following conditions: (vii) 1. mCPBA 2. (viii) 1. O₃ 2. CH₃SCH₃.

(e)

Propose a synthesis of the carbonyl(s) using the (i) ozonolysis pathways.

(a)

Propose a synthesis of the carbonyl(s) using the (i) ozonolysis pathways.

(b)

Draw the product(s) you'd expect when each of these alkenes is treated first with O₃, then with CH₃SCH₃

(d)

Predict the product of ozonolysis of the triglyceride shown.

Predict the product of the following aldehyde/ketone syntheses.

(a) <IMAGE>

Predict the product of the following aldehyde/ketone syntheses.

(a)