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महाराष्ट्र राज्य शिक्षण मंडळएचएससी विज्ञान (सामान्य) इयत्ता १२ वी

Write the correct order of increasing ease of dehydrohalogenation. CHX3−CHX2−CHX2−Cl(I) CHX3−CH(Cl)−CHX3(II) CHX3|CHX3−C−Cl...|CHX3(III) - Chemistry

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प्रश्न

Write the correct order of increasing ease of dehydrohalogenation.

\[\ce{\underset{\text{(I)}}{CH3 - CH2 - CH2 - Cl}}\]

\[\ce{\underset{\text{(II)}}{CH3 - CH(Cl) - CH3}}\]

\[\begin{array}{cc}
\ce{CH3}\\
|\\
\ce{CH3-C-Cl}\phantom{...}\\
|\\
\ce{CH3}\\
\ce{(III)}
\end{array}\]

एका वाक्यात उत्तर
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उत्तर

The correct order of increasing ease of dehydrohalogenation is, III > II > I.

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पाठ 10: Halogen Derivatives - Very Short Answer Questions

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एससीईआरटी महाराष्ट्र Chemistry [English] 12 Standard HSC
पाठ 10 Halogen Derivatives
Very Short Answer Questions | Q 7

संबंधित प्रश्‍न

from the following pair would undergo SN2 faster from the other?

a. CH3CH2CH2I      b. CH3CH2CH2Cl


Complete the following reaction giving major products.

\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]


Complete the following reaction giving major products.

\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]


Complete the following reaction giving major product.

\[\begin{array}{cc}\ce{CH3\phantom{................}}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3\phantom{................}}
\end{array}\]


Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane


Name the reagent used to bring about the following conversion.

1-Chloropropane to 1-nitropropane


Name the reagent used to bring about the following conversion.

Chlorobenzene to biphenyl


Arrange the following in the increasing order of boiling points.

  1. 1-Bromopropane
  2. 2- Bromopropane
  3. 1- Bromobutane
  4. 1-Bromo-2-methylpropane

Give reasons:

Haloarenes are less reactive than haloalkanes.


Convert the following:

Benzyl alcohol to benzyl cyanide


Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.

\[\ce{Isopropyl alcohol ->[\triangle][PBr3] A ->[][NH3 excess] B}\]


Observe the following and answer the question given below.

Comment on the bond length of C–X bond in it.


The following will react faster by SN1 mechanism


Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.


Explain the factors affecting SN1 and SN2 mechanism.


In alkaline hydrolysis of tertiary butyl bromide, ____________.


The least reactive towards nucleophilic addition reactions is ____________.


The following mechanism has been proposed for the reaction of NO2 with F2 to form NO2F:

\[\ce{NO2_{(g)} + F2_{(g)} -> NO2F_{(g)} + F_{(g)} (slow)}\]

\[\ce{F_{(g)} + NO2_{(g)} -> NO2F_{(g)} (fast)}\]

The order of the reaction with respect to NO2(g)


The order of reactivities of the following alkyl halides for an SN2 reaction is ______.


Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?


The order of reactivity of the given haloalkanes towards nucleophiles is:


Observe the following and answer the question given below:

Comment on the bond length of C-X bond in it.


Complete the following reaction sequences by writing the structural formulae of the organic compounds 'A', 'B' and 'C'.

\[\ce{2-Bromobutan ->[alc. KOH] A ->[][Br2] B ->[][NANH2] C}\]


Identify the chiral molecule from the following.


Complete the following reaction giving major product.

\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]


Give a reason for the following:

Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.


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