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What effect does branching of an alkane chain has on its boiling point? - Chemistry

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प्रश्न

What effect does branching of an alkane chain has on its boiling point?

थोडक्यात उत्तर

उत्तर

Alkanes experience inter-molecular Van der Waals forces. The stronger the force, the greater will be the boiling point of the alkane.

As branching increases, the surface area of the molecule decreases which results in a small area of contact. As a result, the Van der Waals force also decreases which can be overcome at a relatively lower temperature. Hence, the boiling point of an alkane chain decreases with an increase in branching.

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Isomerism
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पाठ 13: Hydrocarbons - EXERCISES [पृष्ठ ४०५]

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एनसीईआरटी Chemistry - Part 1 and 2 [English] Class 11
पाठ 13 Hydrocarbons
EXERCISES | Q 13.15 | पृष्ठ ४०५

संबंधित प्रश्‍न

Write IUPAC name of the product obtained by the ozonolysis of the following compound:

3,4-Dimethyl-hept-3-ene


Write IUPAC name of the product obtained by the ozonolysis of the following compound:

2-Ethylbut-1-ene 


Draw the cis and trans structures of hex-2-ene. Which isomer will have higher b.p. and why?


Find out the type of isomerism exhibited by the following pair.

CH3 – CH2 – NH – CH2 - CH3 and CH3 - NH - CH2 - CH2 - CH3


Find out the type of isomerism exhibited by the following pair.


What is the relationship between the members of following pairs of structures? Are they structural or geometrical isomers or resonance contributors?


What is the relationship between the members of following pairs of structures? Are they structural or geometrical isomers or resonance contributors?

\[\begin{array}{cc}\ce{^+OH}\\||\\
\ce{H - C - OH}\end{array}\]

\[\begin{array}{cc}\ce{OH}\phantom{.}\\|\phantom{...}\\
\ce{H - C^+ - OH}\end{array}\]


In which of the following, functional group isomerism is not possible?


Which of the following pairs are position isomers?

I. \[\begin{array}{cc}
\phantom{.......................}\ce{O}\\
\phantom{.......................}||\\
\ce{CH3 - CH2 - CH2 - CH2 - C - H}
\end{array}\]
II. \[\begin{array}{cc}
\phantom{.................}\ce{O}\\
\phantom{.................}||\\
\ce{CH3 - CH2 - CH2 - C - H}
\end{array}\]
III. \[\begin{array}{cc}
\ce{CH3 - CH2 - C - CH2 - CH3}\\
\phantom{}||\\
\phantom{}\ce{O}
\end{array}\]
IV. \[\begin{array}{cc}
\ce{CH3 - CH - CH2 - C - H}\\
\phantom{...}|\phantom{............}||\phantom{}\\
\phantom{...}\ce{CH3}\phantom{.........}\ce{O}\phantom{}
\end{array}\]

(i) I and II

(ii) II and III

(iii) II and IV

(iv) III and IV


Consider structures I to VII and answer the question:

I. CH3 – CH2 – CH2 – CH2 – OH
II. \[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{OH}
\end{array}\]
III. \[\begin{array}{cc}
\phantom{...}\ce{CH3}\\
\phantom{}|\\
\ce{CH3 - C - CH3}\\
\phantom{}|\\
\phantom{..}\ce{OH}
\end{array}\]
IV. \[\begin{array}{cc}
\ce{CH3 - CH - CH2 - OH}\\
|\phantom{........}\\
\ce{CH3}\phantom{......}
\end{array}\]
V. CH3 – CH2 – O – CH2 – CH3
VI. CH3 – O – CH2 – CH2 – CH3
VII. \[\begin{array}{cc}
\ce{CH3 - O - CH - CH3}\\
\phantom{...}|\\
\phantom{......}\ce{CH3}
\end{array}\]

Identify the pairs of compounds that represents position isomerism.


Consider structures I to VII and answer the question:

I. CH3 – CH2 – CH2 – CH2 – OH
II. \[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{OH}
\end{array}\]
III. \[\begin{array}{cc}
\phantom{...}\ce{CH3}\\
\phantom{}|\\
\ce{CH3 - C - CH3}\\
\phantom{}|\\
\phantom{..}\ce{OH}
\end{array}\]
IV. \[\begin{array}{cc}
\ce{CH3 - CH - CH2 - OH}\\
|\phantom{........}\\
\ce{CH3}\phantom{......}
\end{array}\]
V. CH3 – CH2 – O – CH2 – CH3
VI. CH3 – O – CH2 – CH2 – CH3
VII. \[\begin{array}{cc}
\ce{CH3 - O - CH - CH3}\\
\phantom{...}|\\
\phantom{......}\ce{CH3}
\end{array}\]

Identify the pairs of compounds that represents chain isomerism.


Assertion (A): Pent- 1- ene and pent- 2- ene are position isomers.

Reason (R): Position isomers differ in the position of functional group or a substituent.


The molecules having dipole moment are:

(i) 2,2-Dimethylpropane

(ii) trans-Pent-2-ene

(iii) cis-Hex-3-ene

(iv) 2, 2, 3, 3 - Tetramethylbutane.


Tautomerism is exhibited by ______. 


Which of the following does NOT exhibit geometrical isomerism? 


Ether and alcohol are ______.


The compound which shows metamerism is ______


Which type of isomerism can not be shown by benzaldoxime?


Which one of the following pairs are called position isomers?


The correct stereochemical name of


How many structural isomers possible of the molecular formula C3H6O (excluding enol form)?


The number of acyclic structural isomers (including geometrical isomers) for pentene are ______.


Compound with molecular formula C3H6O can show ______.


Which of the following pairs of compounds are positional isomers?


Which of the following reactions will not produce a racemic product?


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