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.

the atomic mass is the bottom number on the element.

-steel jelly

because natural gas is colorless, odorless, and tasteless, distributors add mercaptan (a chemical that smells like sulfur) to give natural gas a distinct unpleasant odor (it smells like rotten eggs). they locate the types of rock that are likely to contain natural gas deposits.