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

Write the structure of the major organic product in the following reaction: CH3CH2CH2OH + SOCl2 ->

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प्रश्न

Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH2CH2OH + SOCl2 ->}\]

रासायनिक समीकरणे/रचना
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उत्तर

\[\ce{\underset{Propan-1-ol}{CH3CH2CH2OH} + SOCl2 ->[nucleophilic substitution] \underset{1-Chloropropane}{CH3CH2CH2Cl} + HCl\uparrow + SO2\uparrow}\]

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पाठ 6: Haloalkanes and Haloarenes - Exercises [पृष्ठ १९०]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 6 Haloalkanes and Haloarenes
Exercises | Q 6.14 (vi) | पृष्ठ १९०

संबंधित प्रश्‍न

Write the main products when methyl chloride is treated with AgCN.


In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?


Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH(Br)CH2CH3 + NaOH ->[water]}\]


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The stability order for carbocation is _______.

(A) 2° > 3° > 1° 

(B) 3° > 2° > 1°

(C) 3° > 1° > 2°

(D) 1° > 3° > 2°


What is the action of the following on ethyl bromide
alcoholic solution of potassium hydroxide.


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moist silver oxide


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(i) The given reaction follows SN2 mechanism.

(ii) (b) and (d) have opposite configuration.

(iii) (b) and (d) have same configuration.

(iv) The given reaction follows SN1 mechanism.


Ethylene chloride and ethylidene chloride are isomers. Identify the correct statements.

(i) Both the compounds form same product on treatment with alcoholic KOH.

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(iii) Both the compounds form same product on reduction.

(iv) Both the compounds are optically active.


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The number of chiral carbons present in the molecule given below is ______.


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CH3Cl, CH3CH2Cl, (CH3)2CHCl and (CH3)3CCl is ______.


Which alkyl halide from the following pair would you expect to react more rapidly by an SN2 mechanism? Explain your answer.

\[\begin{array}{cc}
\ce{CH3CHCH2CH2Br}\\
|\phantom{.............}\\
\ce{CH3}\phantom{..........}\\
\end{array}\] or \[\begin{array}{cc}
\ce{CH3CH2CHCH2Br}\\
|\\
\phantom{...}\ce{CH3}\\
\end{array}\]


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