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Explain the difference in the following ...

Explain the difference in the following reactions.
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When the concentration of the nucleophile `(overset (Ө) O H)` is high `(5N NaOH)`, it follows `SN^2` reaction and inversion takes place.

With dil. `NaOH, SN^1` mechanism is followed when `(C=O)` bond at chircal carbon is cleaved forming a carbonium. Hence, attack by nucleophile `(overset (Ө) O H)` takes place from both directions forming inversion and retention products resulting in `(+-)` forms, i.e., inactive forms.
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CENGAGE CHEMISTRY ENGLISH-ORGANIC REACTION MECHANISM-Subjective
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  2. What are the products and types of isomers when Br2 adds to :

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  3. . identify the product (A)

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  4. Give the stereochemical products of the following : (i) CH-=CH+Br(2)...

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  5. Give the products of the following organic reactions :

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  6. Of the following pairs, which is the faster SN^2 reactions ?

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  7. Of the following pairs, which is the faster SN^1 reactions ? .

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  8. Which of the following would give a better yield of ether ? .

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  9. Give the decreasing order of SN^1 reactions of the following compounds...

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  10. Give the major product when the following compounds are reacted with C...

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  11. 2-Bromopentane is treated with alcoholic KOH solution. Whatt will be t...

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  12. 2-Pentanol can coverted to 2-ethoxy pentane by two paths. In path I, c...

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  13. When reacts with alcoholic KCN, a mixture of isomeric products is ...

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  14. Give the stereochemical products of the following : .

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  15. Give the sterochemical products : HC-=CH + 2NaNH2 + 2EtBr rarr (A) ...

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  16. Identify (B),(c), and (D). .

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  17. . Identify the products

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  18. Explain the difference in the following reactions. .

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  19. Predict the products with configurations in the following. (a) (+)2-...

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