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:
SPECIFIC HEAT CAPACITY
Explanation:
Q = MC DELTA T
q = heat
c = specific heat
T = temperature ( final - initial )
Answer:
true
Explanation:
the more energy a wave has the greater the amplitude is