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yawa3891 [41]
4 years ago
5

Can anybody help me with these 2 ohms law

Chemistry
1 answer:
Fynjy0 [20]4 years ago
3 0

Answer:

1

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Explanation:

Let's break it down:

  • Butane- A 4 carbon alkane
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  • 2,2 - Both the Methyl groups are attached at carbon 2

We can now draw the structure of  2,2-dimethyl butane​ using the following steps:

  1. Draw the backbone (butane)
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d. All of the above three answers are correct

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Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. Use the wedge/hash bond
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See the image 1

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The result of this backside attack is that the stereochemical configuration at the central carbon inverts as the reaction proceeds. In a sense, the molecule is turned inside out. At the transition state, the electrophilic carbon and the three 'R' substituents all lie on the same plane. (see image 3)

What this means is that SN2 reactions whether enzyme catalyzed or not, are inherently stereoselective: when the substitution takes place at a stereocenter, we can confidently predict the stereochemical configuration of the product.

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