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SN^(1) and SN^(2) mechanisms...

`SN^(1)` and `SN^(2)` mechanisms

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### Step-by-Step Solution for SN1 and SN2 Mechanisms **Step 1: Definition of SN1 and SN2 Mechanisms** - **SN1 Mechanism**: This is a nucleophilic substitution reaction that involves a single reactant molecule (unimolecular) in the rate-determining step. The mechanism proceeds through the formation of a carbocation intermediate. - **SN2 Mechanism**: This is a nucleophilic substitution reaction that involves two reactant molecules (bimolecular) in the rate-determining step. The reaction proceeds via a single transition state without the formation of an intermediate. **Step 2: Molecularity and Kinetics** - **SN1**: The molecularity is 1, and it follows first-order kinetics. This means that the rate of the reaction depends only on the concentration of the substrate. ...
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Explain the factors affecting SN_(1) and SN_(2) mechanism.

SN2 Mechanism

The rate of SN^2 reaction depends on the effectiveness of the nucleophile in ejecting the leaving group. Nucleophilicity is the affinity for C atom, while basicity is the affinity for proton. In both cases, a new bond is formed. If a new bond is formed between the anion and proton, the specied acts as a base. If a new bond is formed between the anion and C atom, the species acts as nucleophile. Which of the following compounds gives SN^1, SN^2 , and SN^2 mechanisms ?

a. Given the major products formed by heating the following ethers with conc. HI with metioning SN^(-1) or SN^(-2) mechanism. i. (1- Propoxy propane) ii. Ph--O--Me (Methoxy benzene) iii. Ph--CH_(2)--O--Et (benzyl ethyl ether) iv. (1-Ethoxy-2-methyl butane) v. (2-Propoxy-2-methyl butane) vi. PhCH_(2)OPh (Benzyl phenyl ether) vii. (Tetrahydrofuran, THF) b. Given the products of the above ethers with excess of HI. c. Why does SN^(-2) cleavage occur at a faster rate with HI than with HCI ?

Predicrt the order of reactivity of the following compounds in SN^(1) and SN^(2) reactions.