मराठी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान इयत्ता ११

Consider structures I to VII and answer the question: I. CH3 – CH2 – CH2 – CH2 – OH II. CHX3−CHX2−CH−CHX3.....|.......OH III. ...CHX3|CHX3−C−CHX3|..OH IV. CHX3−CH−CHX2−OH|........CHX3...... - Chemistry

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प्रश्न

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 which are functional group isomers.

टीपा लिहा
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उत्तर

The compounds with the same molecular formula but different functional groups are said to be functional group isomers. 

Alcohols are found to be the functional isomers of ether. In the given structures, I, II, III, IV alcohol functional group is present and V, VI, VII contains ether functional group. Hence, I and V, I and VI, I and VII, II and V, II and VI, II and VII, III and V, III and VI etc are functional group isomers.

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पाठ 12: Organic Chemistry Some Basic Principles and Techniques - Multiple Choice Questions (Type - I) [पृष्ठ १५०]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 11
पाठ 12 Organic Chemistry Some Basic Principles and Techniques
Multiple Choice Questions (Type - I) | Q 24 | पृष्ठ १५०

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?


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

\[\begin{array}{cc}
\ce{D}\phantom{......}\ce{H}\\
\backslash\phantom{......}/\\
\ce{C = C}\\
\phantom{...}/\phantom{......}\backslash\phantom{...}\\\ce{H}\phantom{.......}\ce{D}
\end{array}\]

\[\begin{array}{cc}
\ce{D}\phantom{......}\ce{D}\\
\backslash\phantom{......}/\\
\ce{C = C}\\
\phantom{...}/\phantom{......}\backslash\phantom{...}\\\ce{H}\phantom{.......}\ce{H}\end{array}\]


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.


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


What type(s) of isomerism is(are) shown by [Co(NH3)4Br2]Cl?


But-1-ene and But-2-ene are examples of ____________.


Which of the following is a functional isomer of pentan-2-ol?


The type of isomerism possible in 2-butene is ____________.


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


Which of the following pairs are not functional group 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) II and III

(ii) II and IV

(iii) I and IV

(iv) I and II


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.


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.


The compound which shows metamerism is ______


Acetamide is isomer of ______.


Which one of the following pairs are called position isomers?


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 reactions will not produce a racemic product?


The number of geometrical isomers from [Co(NH3)3(NO2)3] is ______.


Which of the following pairs of compounds is an example of position isomerism?


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