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ozzi
3 years ago
15

Which isomer of 1-bromo-2-tert-butylcyclohexane reacts faster when refluxed with potassium tert-butoxide?Draw the structure of t

he expected major product from the faster reacting compound.
Chemistry
1 answer:
ivolga24 [154]3 years ago
8 0

Answer:

See explanation and image attached

Explanation:

The reaction of 1-bromo-2-tert-butylcyclohexane with  potassium tert-butoxide is an elimination reaction that occurs by E2 mechanism.

The E2 reaction proceeds faster when the hydrogens are in an antiperiplanar position at an angle of 180 degrees.

This is only attainable in the trans isomer of 1-bromo-2-tert-butylcyclohexane. Hence trans 1-bromo-2-tert-butylcyclohexane reacts faster with potassium tert-butoxide

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Vitek1552 [10]

Answer:

See explanation

Explanation:

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Remember that Charles' law states that, the volume of a given mass of gas is directly proportional to its absolute temperature at constant pressure. Since the pressure was held constant, the drop in the volume of gas in the balloon can be accounted for by the drop in temperature overnight.

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3 years ago
Which moon phase does a solar eclipse occur in?
VARVARA [1.3K]

Answer:

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6 0
3 years ago
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<span>E = mCdT
E = energy, m = mass, C = specific heat capacity, dT = change in temperature.
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3 years ago
How many significant digits does the number 700 have?
OLga [1]

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3 years ago
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Answer
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hope this helps and have a wonderful day :)
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