मराठी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

How will you bring about the following conversion? Toluene to benzyl alcohol

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प्रश्न

How will you bring about the following conversion?

Toluene to benzyl alcohol

How the following conversion can be carried out?

Toluene to benzyl alcohol

How will you bring about the following conversion in not more than two steps?

Toluene to Benzyl alcohol

रासायनिक समीकरणे/रचना
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उत्तर १

shaalaa.com

उत्तर २

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  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 6: Haloalkanes and Haloarenes - Exercises [पृष्ठ १९१]

APPEARS IN

एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 6 Haloalkanes and Haloarenes
Exercises | Q 6.19 (iv) | पृष्ठ १९१
एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 6 Haloalkanes and Haloarenes
Exercises | Q 6.11 (iv) | पृष्ठ १९०
नूतन Chemistry [English] Class 12 ISC
पाठ 6 Haloalkanes and Haloarenes
LONG ANSWER TYPE QUESTIONS | Q 16. (iv) | पृष्ठ ६१५

संबंधित प्रश्‍न

How do you convert the following:

Ethanol to propanenitrile


Which compound in the following pair will react faster in SN2 reaction with OH?

(CH3)3CCl or CH3Cl


The treatment of alkyl chlorides with aqueous KOH leads to the formation of alcohols but in the presence of alcoholic KOH, alkenes are major products. Explain.


What is the action of the following on ethyl bromide:
moist silver oxide


In the SN1 reaction, racemization takes place. It is due to:


Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of ____________.


Which of the following is the correct order of decreasing SN2 reactivity?


An organic molecule necessarily shows optical activity if it ____________.


SN1 reaction of alkyl halides lead to ___________.


The increasing order of reactivity towards SN1 mechanism is:

(I) \[\begin{array}{cc}
\ce{CH3-CH-CH2-CH3}\\
|\phantom{........}\\
\ce{CH3}\phantom{.....}
\end{array}\]

(II) CH3CH2CH2Cl

(III) P–CH3O–C6H4–CH2Cl


Cyanide ion acts as an ambident nucleophile. From which end it acts as a stronger nucleophile in aqueous medium? Give reason for your answer.


Why are aryl halides less reactive towards nucleophilic substitution reactions than alkyl halides?


Give reason for the following:

The product formed during SN1 reaction is a racemic mixture.


The major product formed in the following reaction is:


Racemisation occurs in ______.


Inversion of configuration occurs in ______.


 Acetic anhydride from acetic acid


Which of the following reactions is an example of nucleophilic substitution reaction?


Assertion (A): undergoes SN2 reactions faster than .

Reason (R): Iodine is a better leaving group because of its large size.

In the light of the above statements, choose the correct answer from the options given below:


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