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kykrilka [37]
3 years ago
5

Consider the substitution reaction that rakes place when (R)-3-bromo 3-methylhexane is treated with methanol. Which of the follo

wing would be true? The reaction would take place only with inversion of configuration at the center. The reaction would take place only with retention of configuration at the center. The reaction would take place with racemization. No reaction would take place. The alkyl halide does not possess a center.

Chemistry
1 answer:
Otrada [13]3 years ago
5 0

Answer:

The reaction would take place with racemization.

Explanation:

The compound (R)-3-bromo 3-methylhexane contains has the leaving group attached to a tertiary carbon atom. When the leaving group is attached to a tertiary carbon atom, the compound undergoes nucleophilic substitution via SN1 mechanism. This mechanism involves the formation of a planar carbocation intermediate. The nucleophile may attack this intermediate from either faces, leading to racemization of the product.

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Answer:

4.) 9, 1, and 4    5.) 4, 1, and 4

Explanation:

I am not quite sure about this because I cannot remember if the coefficient (the number before the elements) is applied to every element in the compound. If it is then your number of atoms are as follows: CORRECTION: you do not have to apply the coefficient to every element only the one that is after it. So when you back and fix the error your number of atoms will be as follows:

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you can calculate the number of atoms present in this compound by multiplying the coefficient and the subscripts of each atom.

hope this helped you :)

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