For many chemical reactions, the actual yield is usually less than the theoretical yield. This is due to possible loss in the process or inefficiency of the chemical reaction.

4 0

2 years ago

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What does C represent

zimovet [89]

Answer: the distance of energy from point d to e

8 0

3 years ago

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Draw the major organic substitution product(s) for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. Indicate

Andrew [12]

Answer:

(2R,3S)-2-ethoxy-3-methylpentane

and

(2S,3S)-2-ethoxy-3-methylpentane

Explanation:

For this case, we will have $CH_3CH_2O^-$ as nucleophile. Also, this compound is also in excess. So, we will have as solvent $CH_3CH_2OH$ a protic solvent. Therefore the Sn1 reaction would be favored.

The first step would be the carbocation formation followed by the attack of the nucleophile. In this case both isomers would be produced: R and S (see figure).

7 0

2 years ago