Answer:
HCl is not a catalyst because these are not used up during the chemical reactions.
Explanation:
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In this case, according to the performed experiments, it is possible for us to realize that HCl cannot be a catalyst for this reaction because it is used up during the reaction. This is explained by the fact that catalyst are able to return to the original form once the reaction has gone to completion; this is the example of palladium in the hydrogenation or dehydrogenation of hydrocarbons depending on the case. Moreover, we know that the catalysts increase the reaction rate because they decrease the activation energy of the reaction and therefore the student observed such increase.
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Answer:
(2R,3S)-2-ethoxy-3-methylpentane
and
(2S,3S)-2-ethoxy-3-methylpentane
Explanation:
For this case, we will have 
as nucleophile. Also, this compound is also in excess. So, we will have as solvent 
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).
The primary function of chloroplast is to conduct photosynthesis, which is the process plants use to convert light energy into chemical energy that can be released to fuel the organisms' activities.
