232122
Compounds with $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ as molecular formula can exhibit
1 Position isomerism
2 Metamerism
3 Functional isomerism
4 All the three
Explanation:
The possible isomers of $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ are as Thus, it shows all, position isomerism, metamerism and functional isomerism.
JCECE - 2011
GENERAL ORGANIC CHEMISTRY
232124
Among the following which one can have a mesoform?
(B) : Compound (b) have plane of symmetry thus it has meso form.
JCECE - 2013
GENERAL ORGANIC CHEMISTRY
232186
In assigning R-S configuration, which among the following groups has highest priority?
1 $-\mathrm{SO}_{3} \mathrm{H}$
2 $-\mathrm{COOH}$
3 $-\mathrm{CHO}$
4 $-\mathrm{C}_{6} \mathrm{H}_{5}$
Explanation:
In this question priority order decided on the basis of - Atomic Number - Mass Number In this groups sulpher atom has highest Atomic No. So priority will be high for $\mathrm{SO}_{3} \mathrm{H}$.
MHT CET-2017
GENERAL ORGANIC CHEMISTRY
232126
Which of the following acids does not exhibit optical isomerism?
1 Tartaric acid
2 Lactic acid
3 Maleic acid
4 $\alpha$-amino acids
Explanation:
Structure of these acids are All of these acids except maleic acid have at least one chiral carbon $\left(^{*}\right)$ hence these are optically active but maleic acid is not.
JCECE - 2017
GENERAL ORGANIC CHEMISTRY
232130
The structures of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left[\mathrm{CH}_{2}\right]_{3} \mathrm{Br}$ represent
1 Chain isomerism
2 Position isomerism
3 Chain as well as position isomerism
4 Functional isomerism
Explanation:
The structure of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{3}$ $\mathrm{Br}$ Position of functional group is change. So, it is also a position isomer. Chain as well as position isomer is correct isomerism
232122
Compounds with $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ as molecular formula can exhibit
1 Position isomerism
2 Metamerism
3 Functional isomerism
4 All the three
Explanation:
The possible isomers of $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ are as Thus, it shows all, position isomerism, metamerism and functional isomerism.
JCECE - 2011
GENERAL ORGANIC CHEMISTRY
232124
Among the following which one can have a mesoform?
(B) : Compound (b) have plane of symmetry thus it has meso form.
JCECE - 2013
GENERAL ORGANIC CHEMISTRY
232186
In assigning R-S configuration, which among the following groups has highest priority?
1 $-\mathrm{SO}_{3} \mathrm{H}$
2 $-\mathrm{COOH}$
3 $-\mathrm{CHO}$
4 $-\mathrm{C}_{6} \mathrm{H}_{5}$
Explanation:
In this question priority order decided on the basis of - Atomic Number - Mass Number In this groups sulpher atom has highest Atomic No. So priority will be high for $\mathrm{SO}_{3} \mathrm{H}$.
MHT CET-2017
GENERAL ORGANIC CHEMISTRY
232126
Which of the following acids does not exhibit optical isomerism?
1 Tartaric acid
2 Lactic acid
3 Maleic acid
4 $\alpha$-amino acids
Explanation:
Structure of these acids are All of these acids except maleic acid have at least one chiral carbon $\left(^{*}\right)$ hence these are optically active but maleic acid is not.
JCECE - 2017
GENERAL ORGANIC CHEMISTRY
232130
The structures of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left[\mathrm{CH}_{2}\right]_{3} \mathrm{Br}$ represent
1 Chain isomerism
2 Position isomerism
3 Chain as well as position isomerism
4 Functional isomerism
Explanation:
The structure of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{3}$ $\mathrm{Br}$ Position of functional group is change. So, it is also a position isomer. Chain as well as position isomer is correct isomerism
232122
Compounds with $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ as molecular formula can exhibit
1 Position isomerism
2 Metamerism
3 Functional isomerism
4 All the three
Explanation:
The possible isomers of $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ are as Thus, it shows all, position isomerism, metamerism and functional isomerism.
JCECE - 2011
GENERAL ORGANIC CHEMISTRY
232124
Among the following which one can have a mesoform?
(B) : Compound (b) have plane of symmetry thus it has meso form.
JCECE - 2013
GENERAL ORGANIC CHEMISTRY
232186
In assigning R-S configuration, which among the following groups has highest priority?
1 $-\mathrm{SO}_{3} \mathrm{H}$
2 $-\mathrm{COOH}$
3 $-\mathrm{CHO}$
4 $-\mathrm{C}_{6} \mathrm{H}_{5}$
Explanation:
In this question priority order decided on the basis of - Atomic Number - Mass Number In this groups sulpher atom has highest Atomic No. So priority will be high for $\mathrm{SO}_{3} \mathrm{H}$.
MHT CET-2017
GENERAL ORGANIC CHEMISTRY
232126
Which of the following acids does not exhibit optical isomerism?
1 Tartaric acid
2 Lactic acid
3 Maleic acid
4 $\alpha$-amino acids
Explanation:
Structure of these acids are All of these acids except maleic acid have at least one chiral carbon $\left(^{*}\right)$ hence these are optically active but maleic acid is not.
JCECE - 2017
GENERAL ORGANIC CHEMISTRY
232130
The structures of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left[\mathrm{CH}_{2}\right]_{3} \mathrm{Br}$ represent
1 Chain isomerism
2 Position isomerism
3 Chain as well as position isomerism
4 Functional isomerism
Explanation:
The structure of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{3}$ $\mathrm{Br}$ Position of functional group is change. So, it is also a position isomer. Chain as well as position isomer is correct isomerism
232122
Compounds with $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ as molecular formula can exhibit
1 Position isomerism
2 Metamerism
3 Functional isomerism
4 All the three
Explanation:
The possible isomers of $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ are as Thus, it shows all, position isomerism, metamerism and functional isomerism.
JCECE - 2011
GENERAL ORGANIC CHEMISTRY
232124
Among the following which one can have a mesoform?
(B) : Compound (b) have plane of symmetry thus it has meso form.
JCECE - 2013
GENERAL ORGANIC CHEMISTRY
232186
In assigning R-S configuration, which among the following groups has highest priority?
1 $-\mathrm{SO}_{3} \mathrm{H}$
2 $-\mathrm{COOH}$
3 $-\mathrm{CHO}$
4 $-\mathrm{C}_{6} \mathrm{H}_{5}$
Explanation:
In this question priority order decided on the basis of - Atomic Number - Mass Number In this groups sulpher atom has highest Atomic No. So priority will be high for $\mathrm{SO}_{3} \mathrm{H}$.
MHT CET-2017
GENERAL ORGANIC CHEMISTRY
232126
Which of the following acids does not exhibit optical isomerism?
1 Tartaric acid
2 Lactic acid
3 Maleic acid
4 $\alpha$-amino acids
Explanation:
Structure of these acids are All of these acids except maleic acid have at least one chiral carbon $\left(^{*}\right)$ hence these are optically active but maleic acid is not.
JCECE - 2017
GENERAL ORGANIC CHEMISTRY
232130
The structures of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left[\mathrm{CH}_{2}\right]_{3} \mathrm{Br}$ represent
1 Chain isomerism
2 Position isomerism
3 Chain as well as position isomerism
4 Functional isomerism
Explanation:
The structure of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{3}$ $\mathrm{Br}$ Position of functional group is change. So, it is also a position isomer. Chain as well as position isomer is correct isomerism
232122
Compounds with $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ as molecular formula can exhibit
1 Position isomerism
2 Metamerism
3 Functional isomerism
4 All the three
Explanation:
The possible isomers of $\mathrm{C}_{4} \mathrm{H}_{11} \mathrm{~N}$ are as Thus, it shows all, position isomerism, metamerism and functional isomerism.
JCECE - 2011
GENERAL ORGANIC CHEMISTRY
232124
Among the following which one can have a mesoform?
(B) : Compound (b) have plane of symmetry thus it has meso form.
JCECE - 2013
GENERAL ORGANIC CHEMISTRY
232186
In assigning R-S configuration, which among the following groups has highest priority?
1 $-\mathrm{SO}_{3} \mathrm{H}$
2 $-\mathrm{COOH}$
3 $-\mathrm{CHO}$
4 $-\mathrm{C}_{6} \mathrm{H}_{5}$
Explanation:
In this question priority order decided on the basis of - Atomic Number - Mass Number In this groups sulpher atom has highest Atomic No. So priority will be high for $\mathrm{SO}_{3} \mathrm{H}$.
MHT CET-2017
GENERAL ORGANIC CHEMISTRY
232126
Which of the following acids does not exhibit optical isomerism?
1 Tartaric acid
2 Lactic acid
3 Maleic acid
4 $\alpha$-amino acids
Explanation:
Structure of these acids are All of these acids except maleic acid have at least one chiral carbon $\left(^{*}\right)$ hence these are optically active but maleic acid is not.
JCECE - 2017
GENERAL ORGANIC CHEMISTRY
232130
The structures of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left[\mathrm{CH}_{2}\right]_{3} \mathrm{Br}$ represent
1 Chain isomerism
2 Position isomerism
3 Chain as well as position isomerism
4 Functional isomerism
Explanation:
The structure of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CBr}$ and $\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{3}$ $\mathrm{Br}$ Position of functional group is change. So, it is also a position isomer. Chain as well as position isomer is correct isomerism
