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

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

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प्रश्न

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.

टीपा लिहा
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उत्तर

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

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

Explanation:

\[\ce{\underset{(ethylidence chloride)}{H3C - CHCl2}}\]  and \[\begin{array}{cc}
\phantom{}\ce{H2C - CH2}\phantom{}\\
\phantom{}|\phantom{....}|\\
\phantom{.}\ce{\underset{(ethylene dichloride)}{\phantom{}Cl\phantom{...}Cl}}\phantom{}
\end{array}\]  are isomers.

(i) They give ethyne on treatment with alcoholic KOH.

\[\ce{CH3CHCl2 ->[alc][KOH] CH ≡ CH + 2KCl + 2H2O}\]

\[\ce{Cl - CH2 - CH2 - Cl ->[alc.KOH] CH ≡ CH + 2KCl + H2O}\]

(ii) On reduction with Zn dust in alcohol they give ethylene.

\[\ce{CH3CHCl2 + Zn ->[CH3OH] CH2 ≡ CH}\]

\[\ce{Cl - CH2 - CH2 - Cl + Zn ->[CH3OH] CH2 = CH2}\]

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पाठ 10: Haloalkanes and Haloarenes - Exercises [पृष्ठ १४१]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
पाठ 10 Haloalkanes and Haloarenes
Exercises | Q II. 38. | पृष्ठ १४१

संबंधित प्रश्‍न

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

CH3CH2CH2CH2Br or \[\begin{array}{cc}
\ce{CH3CH2CHCH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{Br}\ 
\end{array}\]


What are ambident nucleophiles? Explain with an example.


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

\[\ce{CH3CH2Br + KCN ->[aq{.} ethanol]}\]


Arrange the compounds of the following set in order of reactivity towards SN2 displacement:

1-Bromobutane, 1-Bromo-2, 2-dimethylpropane, 1-Bromo-2-methylbutane, 1-Bromo-3-methylbutane


What happens when chlorobenzene is subjected to hydrolysis?


SN1 reactions are accompanied by racemization in optically active alkyl halides.


Which of the following pairs is/are correctly matched?

  Reaction Product
I RX + AgCN RNC
II RX + KCN RCN
III RX + KNO2 \[\begin{array}{cc}
\phantom{.......}\ce{O}\\
\phantom{.....}/\\
\ce{R - N}\phantom{....}\\
\phantom{.....}\backslash\backslash\\
\phantom{.......}\ce{O}
\end{array}\]
IV RX + AgNO2 \[\ce{R-O-N=O}\]

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


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


Which of the following is an optically active compound?


Identify the end product (C) in the following sequence:

\[\ce{C2H5OH ->[SOCl2][Pyridine] A ->[KCN {(alc.)}] B ->[2H2O/H^+] C}\]


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


A primary alkyl halide would prefer to undergo ______.


Compound ‘A’ with molecular formula \[\ce{C4H9Br}\] is treated with aq. \[\ce{KOH}\] solution. The rate of this reaction depends upon the concentration of the compound ‘A’ only. When another optically active isomer ‘B’ of this compound was treated with aq. \[\ce{KOH}\] solution, the rate of reaction was found to be dependent on concentration of compound and \[\ce{KOH}\] both.

(i) Write down the structural formula of both compounds ‘A’ and ‘B’.

(ii) Out of these two compounds, which one will be converted to the product with inverted configuration.


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


Match the reactions given in Column I with the types of reactions given in Column II.

  Column I Column II
(i) (a) Nucleophilic aromatic substitution
(ii) \[\begin{array}{cc}
\ce{CH3 - CH = CH2 + HBr -> CH3 - CH - CH3}\\
\phantom{............................}|\phantom{}\\
\phantom{.............................}\ce{Br}\phantom{}
\end{array}\]
(b) Electrophilic aromatic substitution
(iii) (c) Saytzeff elimination
(iv) (d) Electrophilic addition
(v) \[\begin{array}{cc}
\ce{CH3  CH2 CH CH3 ->[alc.KOH] CH3  CH = CH CH3}\\
\phantom{}|\phantom{..........................}\\
\phantom{}\ce{Br}\phantom{........................}
\end{array}\]
(e) Nucleophilic substitution (SN1)

Which of the following is the definition of chirality?


Which one is the correct order of nucleophilic strength (pKa) of following nucleophiles?


The decreasing order of reactivity of the following compounds towards nucleophilic substitution (SN2) is ______.






Discuss the mechanism of alkaline hydrolysis of methyl bromide.


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