Draw a structure for the product of nucleophilic substitution obtained on solvolysis of tert−butyl bromide in methanol, and arra
nge the correct mechanism for its formation. Be sure to answer all parts.
1 answer:
Answer:
2-methoxy-2-methylpropane
Explanation:
The first step for this reaction is the carbocation formation. In this step, a tertiary carbocation is formed. Also, we will have a good leaving group so bromide will be formed. Then the methanol acts as a nucleophile and attacks the carbocation. Next, a positive charge is generated upon the oxygen, this charge can be removed when the hydrogen leaves the molecule as . (See figure)
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Answer:
The Michaelis‑Menten equation is given as
v₀ = Kcat X [E₀] X [S] / (Km + [S])
where,
Kcat is the experimental rate constant of the reaction; [s] is the substrate concentration and
Km is the Michaelis‑Menten constant.
Explanation:
See attached image for a detailed explanation
