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).
<span>Temperature is defined as the rate at which molecules move or vibrate
</span>
Answer:
0.00000045 m is the wavelength of blue light in decimal
