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When a nucleophile encounters a ketone, ...

When a nucleophile encounters a ketone, the site of attack is :

A

the carbon atom of the carbonyl

B

the oxygen atom of the carbonyl

C

both the carbon and oxygen atoms, with equal probability

D

no attack occurs as ketones do not react with nucleophiles

Text Solution

Verified by Experts

The correct Answer is:
A

`R-underset(deltao+)overset(O)overset(||)(C)-R` more positive on carbon of carbonyl.
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SN^1 reaction is given by alkylhalide which forms stable carbocation during reaction. The carbonation, has sp^2 hybridisation. In SN^1 reaction, the attack of the nucleophile to carbocation inter mediate is from either side. In SN^2 reaction the attacking nucleophile attacks from the back leading to the formation of inversion complex. Alcohol reacts with PCI_5 to give alkyl chloride by an internal attack of nucleophile with in the molecule. In the following reaction

SN^1 reaction is given by alkylhalide which forms stable carbocation during reaction. The carbonation, has sp^2 hybridisation. In SN^1 reaction, the attack of the nucleophile to carbocation inter mediate is from either side. In SN^2 reaction the attacking nucleophile attacks from the back leading to the formation of inversion complex. Alcohol reacts with PCI_5 to give alkyl chloride by an internal attack of nucleophile with in the molecule. In the following reaction

SN^1 reaction is given by alkylhalide which forms stable carbocation during reaction. The carbonation, has sp^2 hybridisation. In SN^1 reaction, the attack of the nucleophile to carbocation inter mediate is from either side. In SN^2 reaction the attacking nucleophile attacks from the back leading to the formation of inversion complex. Alcohol reacts with PCI_5 to give alkyl chloride by an internal attack of nucleophile with in the molecule. In the following reaction . If R is H - undersetoverset(|)(D)oversetunderset(|)(CH_3)(C ) - R - OH underset(Py)overset(SOCl_2)(to) R - Cl + SO_2 + HCl

MS CHOUHAN-ALDEHYDES AND KETONES-LEVEL-2
  1. When a nucleophile encounters a ketone, the site of attack is :

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  2. Select the best choice for example (A to L) from the examples (a to n)...

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  3. The following questions refer to the compounds (A to G) shown below :

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  4. Match of the column :

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  5. Complete the following table.

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  6. Consider the following reactions and answer A and B. Suggest a re...

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  7. Yield of each step as actually carried out in the laboratory is given ...

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  8. Degree of unsaturation present in compound (A + B + C) is ?

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  9. Within each set, which compound should be more reactive toward carbony...

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  10. Match the Column (I) and Column (II). (Matrix)

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  11. Consider reactions A through F. Those carbon atoms undergoing change, ...

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  12. Consider the possible formation of an aldehyde or ketone product when ...

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  13. Wittig reaction : The reaction of a phosphorus ylide with an aldehyd...

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  14. Wittig reaction : The reaction of a phosphorus ylide with an aldehyd...

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  15. Wittig reaction : The reaction of a phosphorus ylide with an aldehyd...

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  16. Wittig reaction : The reaction of a phosphorus ylide with an aldehyd...

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  17. Wittig reaction : The reaction of a phosphorus ylide with an aldehyd...

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  18. Wittig reaction : The reaction of a phosphorus ylide with an aldehyd...

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  19. Match the column :

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  20. Reactant (A) is :

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  21. Product (B) is :

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