3. Rate of Sy2 will be negligible in : Br Br Br Br (а) (b) || (c) (d)

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**Question 3:** The rate of \( S_N2 \) will be negligible in:

**Options:**

(a) A bromocyclohexane structure where bromine (Br) is attached to a cyclohexane ring.

(b) A bromocyclohexene structure where bromine (Br) is attached to a cyclohexene ring with one double bond.

(c) A bromonorbornane structure where bromine (Br) is attached to a norbornane framework with marked strain.

(d) A bromocyclohexene structure where bromine (Br) is attached to a cyclohexene ring with one double bond, but with a different arrangement compared to (b).

**Explanation of the Chemical Structures:**

- Each option represents a chemical structure with bromine attached to a carbon ring.
- **(a)** shows a saturated cyclohexane ring with no double bonds, which is less hindered.
- **(b)** illustrates the presence of a double bond in the cyclohexane ring, introducing some degree of ring strain.
- **(c)** highlights the norbornane structure that is known for its significant ring strain, affecting the reaction probability.
- **(d)** includes a double bond similar to **(b)** but with altered sterics, potentially influencing reactivity.

The focus here is to determine the structural scenario where the \( S_N2 \) reaction rate would be least favored due to steric hindrance or electronic effects.
Transcribed Image Text:**Question 3:** The rate of \( S_N2 \) will be negligible in: **Options:** (a) A bromocyclohexane structure where bromine (Br) is attached to a cyclohexane ring. (b) A bromocyclohexene structure where bromine (Br) is attached to a cyclohexene ring with one double bond. (c) A bromonorbornane structure where bromine (Br) is attached to a norbornane framework with marked strain. (d) A bromocyclohexene structure where bromine (Br) is attached to a cyclohexene ring with one double bond, but with a different arrangement compared to (b). **Explanation of the Chemical Structures:** - Each option represents a chemical structure with bromine attached to a carbon ring. - **(a)** shows a saturated cyclohexane ring with no double bonds, which is less hindered. - **(b)** illustrates the presence of a double bond in the cyclohexane ring, introducing some degree of ring strain. - **(c)** highlights the norbornane structure that is known for its significant ring strain, affecting the reaction probability. - **(d)** includes a double bond similar to **(b)** but with altered sterics, potentially influencing reactivity. The focus here is to determine the structural scenario where the \( S_N2 \) reaction rate would be least favored due to steric hindrance or electronic effects.
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