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Arrange the following in the increasing order of boiling points. 1-Bromopropane 2- Bromopropane 1- Bromobutane 1-Bromo-2-methylpropane - Chemistry

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प्रश्न

Arrange the following in the increasing order of boiling points.

  1. 1-Bromopropane
  2. 2- Bromopropane
  3. 1- Bromobutane
  4. 1-Bromo-2-methylpropane
एका वाक्यात उत्तर

उत्तर

1-bromo-2-methylpropane < 2- Bromopropane

< 1-Bromopropane < 1- Bromobutane

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पाठ 10: Halogen Derivatives - Exercises [पृष्ठ २३३]

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बालभारती Chemistry [English] 12 Standard HSC
पाठ 10 Halogen Derivatives
Exercises | Q 2. vii. | पृष्ठ २३३

संबंधित प्रश्‍न

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

a.     b.


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

a. CH3CH2CH2I      b. CH3CH2CH2Cl


Complete the following reaction giving major products.

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


Name the reagent used to bring about the following conversion.

1-Chloropropane to 1-nitropropane


Distinguish between SN1 and SN2 mechanism of substitution reaction.


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

\[\ce{2-Bromobutane->[Alc.KOH]A->[][Br2]B->[][NaNH2]C}\]


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.


Propane nitrile can be prepared by heating ____________


The following will react faster by SN1 mechanism


Explain. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.


In alkaline hydrolysis of tertiary butyl bromide, ____________.


Which of the following is least reactive towards SN1 reactions?


Which of the following is least reactive towards nucleophilic addition?


What type of hybridisation is present in carbocation formed during the alkaline hydrolysis of 1- bromo-1- phenyl ethane?


Convert the following.

p-Nitrochlorobenzene to p-nitrophenol


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


The compound that reacts the fastest with sodium methoxide is ______.


Complete the following reaction giving major products.

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


Observe the following and answer the question given below:

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


Discuss β - elimination reaction.


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.


Complete the following reaction giving major product.

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


Complete the following reaction giving major product.

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


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