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Monica [59]
3 years ago
10

Draw the product formed by the reaction of t-butoxide with (1r,2s)-1-bromo-2-methyl-1-phenylbutane (shown below). (draw the corr

ect stereoisomer of the product.)

Chemistry
2 answers:
zepelin [54]3 years ago
7 0

https://goo.gl/images/Zs316J go here to get the anwser you are looking for.

Vlad [161]3 years ago
6 0

Answer:

(E)-(2-methylbut-1-en-1-yl)benzene

Explanation:

This reaction is an E2 elimination reaction, it involves a single-step mechanism. In the single step mechanism, the required geometry is an anti-peri-planar geometry. In other words, the required configuration is a configuration for the leaving group and the H that would be removed. The leaving group and the hydrogen must now be of an opposite configuration when the base attacks the hydrogen.

Hence the stereo chemistry of the product (E)-(2-methylbut-1-en-1-yl)benzene shown below.

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Burning 10g of propane produces twice as much carbon dioxide as burning 5g of propane what law does it apply?
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What does Le Châtelier's principle state?
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Answer:

B. A reaction at equilibrium will respond to balance a change.

Explanation:

The Le Chatelier's principle states that a reaction will respond to balance a change. This is true for a reaction in chemical equilibrium.

Le Chatelier's principle sates that "if any conditions of a system in equilibrium is changed, the system will adjust itself in order to annul the effect of the change".

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Write out the BALANCED NET IONIC equation for the neutralization reaction that occurs between aqueous phosphoric acid and aqueou
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Explanation:

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