A synthesis would be A+B-->AB its combining, decomposition is AB-->A+B, its the breaking up of a substance.
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).
Answer:
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I believe this question has the following five choices to
choose from:
>an SN2 reaction has occurred with inversion of
configuration
>racemization followed by an S N 2 attack
>an SN1 reaction has taken over resulting in inversion
of configuration
>an SN1 reaction has occurred due to carbocation
formation
>an SN1 reaction followed by an S N 2 “backside”
attack
The correct answer is:
an SN1 reaction has occurred due to carbocation formation
Answer:
Nuclear Fission.
Explanation:
This happens when a high-energy particle collides with a radioisotope, which splits into 2 daughter nuclei, several neutrons (which can collide with more radioisotopes to cause a chain reaction); and a lot of energy. That's why nuclear power plants are so good.
