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Soloha48 [4]
3 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]3 years ago
6 0

Answer:

use google and use the first link

Explanation:

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If iodine-131 has a half-life of 8 days, how much of a 64.0 g sample of iodine-131 will remain after 32 day?
Mariulka [41]

Answer:

4 g OF IODINE-131 WILL REMAIN AFTER 32 DAYS.

Explanation:

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c

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