Explanation:
Tollens' reagent is prepared by using two-step process : -
Step 1:
Silver oxide is formed by mixing aqueous silver nitrate with base like sodium hydroxide. The reaction is shown below as:

Step 2
Ammonia solution is drop-wise added until all the silver oxide dissolves to form the reagent. The reaction is shown below as:

The formation of aspirin will proceed faster if acetic anhydride is used in place of acetic acid.
However, acetic anhydride will hydrolyze in the presence of water to form acetic acid, slowing down the reaction.
Answer:
(1) Bromination, (2) E2 elimination and (3) epoxidation
Explanation:
- In the first step, -OH group in cyclopentanol is replaced by more facile leaving group Br by treating cyclopentanol with

- In the second step, E2 elimination in presence of strong base e.g. NaOEt/EtOH produce cyclopentene
- In the third step, treatment of cyclopentene with mCPBA produces 1,2-epoxycyclopentane
- Full reaction scheme has been shown below