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

Write the structures and names of the compounds formed when compound ‘A’ with molecular formula, CX7HX8 is treated with ClX2 in the presence of FeClX3. - Chemistry

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प्रश्न

Write the structures and names of the compounds formed when compound ‘A’ with molecular formula, \[\ce{C7H8}\] is treated with \[\ce{Cl2}\] in the presence of \[\ce{FeCl3}\].

टीपा लिहा
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उत्तर

The compound with molecular formula \[\ce{C7H8}\] is toluene, \[\ce{C6H5CH3}\]. Since \[\ce{^-CH3}\] group is o-, p-directing, therefore, chlorination of toluene gives o-chlorotoluene and p-chlorotoluene, in which the p-isomer predominates.

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  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 10: Haloalkanes and Haloarenes - Exercises [पृष्ठ १४३]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 12
पाठ 10 Haloalkanes and Haloarenes
Exercises | Q III. 56. | पृष्ठ १४३

संबंधित प्रश्‍न

Which would undergo SN1 reaction faster in the following pair and why?


 Give reasons for the following:

(CH3)3C–O–CH3 on reaction with HI gives (CH3)3C–I and CH3–OH as the main products and not (CH3)3C–OH and CH3–I.


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.


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


What is the action of the following on ethyl bromide?

silver acetate


Most reactive halide towards SN1 reaction is ____________.


SN2 mechanism proceeds through intervention of ____________.


Which among MeX, RCH2X, R2CHX and R3CX is most reactive towards SN2 reaction?


Identify X and Y in the following sequence:

\[\ce{C2H5Br ->[X] Product ->[Y] C3H7NH2}\]


The correct order of increasing the reactivity of C–X bond towards nucleophile in following compounds.


    (I)


     (II)

(CH3)3CCl
    (III)

(CH3)2CHCl
    (IV)


Which of the following compound will undergo racemisation when reacts with aq. KOH?

(i)

(ii)

CH3CH2CH2Cl

(iii)

\[\begin{array}{cc}
\ce{CH3}\phantom{..}\\
|\phantom{....}\\
\ce{CH3-CH-CH2Cl}
\end{array}\]

(iv)

\[\begin{array}{cc}
\phantom{..}\ce{H}\\
\phantom{..}|\\
\ce{CH3-C-Cl}\\
\phantom{..}|\\
\phantom{.....}\ce{C2H5}
\end{array}\]


Which of the following statements are correct about this reaction?

(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.

(ii) Both the compounds form same product on treatment with aq.NaOH.

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

(iv) Both the compounds are optically active.


Chlorination of alkanes is an example of


In which reaction mechanism carbocation is formed?


The major product formed in the following reaction is:


Explain why Grignard reagents should be prepared under anhydrous conditions.


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