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Soloha48 [4]
2 years ago
11

Treatment of (S)-( )-5-methyl-2-cyclohexenone with lithium dimethylcuprate gives, after protonolysis, a good yield of a mixture

containing mostly a dextrorotatory ketone A and a trace of an optically inactive isomer B. Treatment of A with zinc amalgam and HCl affords an optically active, dextrorotatory hydrocarbon C. Identify compounds A, B, and C, including stereochemical configurations. Be sure to explicitly draw H and both wedge/dash bonds at any configuration center.
Chemistry
1 answer:
tekilochka [14]2 years ago
6 0

Answer:

use google and use the first link

Explanation:

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Lera25 [3.4K]

The  statement  which is true is

metals  lose  electrons  to become cations

<u><em>Explanation</em></u>

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PLEASE HELP!!! CHEMISTRY
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