The target diol is synthesized in one step from 1-methylcyclopentene, but your lab partner exhausted the supply of that alkene. fortunately, you have plenty of isomers (c6h10) on hand from which to synthesize 1-methylcyclopentene and, ultimately, the diol. provide the missing reagents and organic structures needed to most efficiently produce the target product.

The reagents are .

Explanation:

1-Methylenecyclopentene is treated with HBr form 1-bromo-1-methylcyclopentane, which is treated with strong base ethoxide ion and forms 1-methylcyclopent-1-ene.

This alkene is treated with osmium tetraoxide in the presence of sodium bisulfite to form target product.

The chemical reaction is as follows.

c. because step up transformer steps up the input voltage i.e increases the input voltage  

the number of turns are greater on the secondary side of step up transformer  

transformer does not handle dc current