I think B. As an idea is just a way that could be possible
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
<span>PV=nRT= a universal constant
For any condition
P1V1/n1T1=R
and
P2V2/n2T2=R
i.e
P1V1/n1T1=P2V2/n2T2
Becomes
V1/n1=V2/n2
rearranging and solving
V2=V1X(n2/n1)= 750 mLx((0.65+0.35)/(0.65))=1200ml=1.2L...2 sig figs</span>