Add curved arrows to the reactant side of the following SN1 mechanism. Add curved arrows to…
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Question “Add curved arrows to the reactant side of the following SN1 mechanism. Add curved arrows to…”
Add curved arrows to the reactant side of the following SN1
mechanism.
Answer
A nucleophilic substitution reaction is the S N1 reaction. The number 1 is unimolecular. This reaction takes place in two steps. The first step is when the substrate’s leaving group separates from the substrate, forming a carbocation. The second step is where the attacking nucleophile attacks the carbocation from the product.
S 1 is for substitution, unimolecular, nucleophilic. One nucleophile can be substituted with another in the S N1 reaction. It’s a two-step process.
The substrate concentration is the only determinant of the rate of reaction. It doesn’t depend on the amount of nucleophile that is incoming.
A nucleophile refers to a molecule, ion or substance that can give an electron pair.
Part 1
For the first step, use the curved arrow mechanism:
![CH3
CH3
-
--
+
+
:B
H3C-
HC
CH3
CH;](https://drive.google.com/uc?id=1xzJHA3EsP3kVExOspQabjyTvAeX2Dl8x&export=download/Add-curved-arrows-to-the-reactant-side-of-the-following-SN1-mechanism.-Add-curved-arrows-to.png?x-oss-process=image/resize,w_560/format,webp)
Part 2
For the first step, use the curved arrow mechanism:
![CH
CH3
HC-
+
+
:
HC
CH3
CHZ](https://drive.google.com/uc?id=1vIfyG5aT6TBb6HeEtLrSQbRXYpm1YHcy&export=download/Add-curved-arrows-to-the-reactant-side-of-the-following-SN1-mechanism.-Add-curved-arrows-to.png?x-oss-process=image/resize,w_560/format,webp)
Part 1: Ans
![CH3
CH3
-
--
+
+
:B
H3C-
HC
CH3
CH;](https://drive.google.com/uc?id=1xzJHA3EsP3kVExOspQabjyTvAeX2Dl8x&export=download/Add-curved-arrows-to-the-reactant-side-of-the-following-SN1-mechanism.-Add-curved-arrows-to.png?x-oss-process=image/resize,w_560/format,webp)
Conclusion
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