The compound which has restricted rotation around carbon-carbon double bond and substituent attached to alkene must be different if it satisfy these condition the molecule exhibit geometrical isomer For the show enantiomerism it must have asymmetric center with non-superimposable mirror image and also it does not place of symmetry. Those molecule exhibit is show both geometrical and enantiomerism In compound (d) it has both restricted rotation as well as a symmetric center
UPTU/ UPSEE-2016
GENERAL ORGANIC CHEMISTRY
232228
A solution of D-glucose in water rotates the plane of polarised light
1 to the left
2 to the right
3 to either side
4 None of these
Explanation:
We know that glucose is optical active compound because it has more than one asymmetric center so it show optical active which rotate the plane polarized light in either leuollelt for dextro direction It is a natural glucose Natural glucose is dextro rotator (Clockwise) and this glucose is known as dextrose. Thus it rotate the plane polarized light to the right in water.
UPTU/ UPSEE-2015
GENERAL ORGANIC CHEMISTRY
232230
A compound contains two dissimilar asymmetric $\mathrm{C}$-atoms. The number of optical isomers is
1 1
2 2
3 4
4 8
Explanation:
A compound have two asymmetric center ie chiral center in which carbon is $\mathrm{sp}^{3}$ hybridised with different subsistent then the Number of optical isomer $=2^{n}$ Where $n$ is chiral center of carbon atom $=2^{\mathrm{n}}=2^{2}=4$ optical isomer
UPTU/ UPSEE-2014
GENERAL ORGANIC CHEMISTRY
232233
Cyclohexane, methylcyclopentane, 1, 3dimethyl cyclobutane and 1, 2, 3-trimethyl cyclopropane are examples of which one of the following?
1 Constitutional isomers
2 Positional isomers
3 Structural isomers
4 Structural as well as positional isomers
Explanation:
,c) Exp: (A,C) : Structural isomers of $\mathrm{C}_{6} \mathrm{H}_{12}$ are. Structural isomer or constitutional isomers are compoundhaving same molecular formula but different structural formula.
The compound which has restricted rotation around carbon-carbon double bond and substituent attached to alkene must be different if it satisfy these condition the molecule exhibit geometrical isomer For the show enantiomerism it must have asymmetric center with non-superimposable mirror image and also it does not place of symmetry. Those molecule exhibit is show both geometrical and enantiomerism In compound (d) it has both restricted rotation as well as a symmetric center
UPTU/ UPSEE-2016
GENERAL ORGANIC CHEMISTRY
232228
A solution of D-glucose in water rotates the plane of polarised light
1 to the left
2 to the right
3 to either side
4 None of these
Explanation:
We know that glucose is optical active compound because it has more than one asymmetric center so it show optical active which rotate the plane polarized light in either leuollelt for dextro direction It is a natural glucose Natural glucose is dextro rotator (Clockwise) and this glucose is known as dextrose. Thus it rotate the plane polarized light to the right in water.
UPTU/ UPSEE-2015
GENERAL ORGANIC CHEMISTRY
232230
A compound contains two dissimilar asymmetric $\mathrm{C}$-atoms. The number of optical isomers is
1 1
2 2
3 4
4 8
Explanation:
A compound have two asymmetric center ie chiral center in which carbon is $\mathrm{sp}^{3}$ hybridised with different subsistent then the Number of optical isomer $=2^{n}$ Where $n$ is chiral center of carbon atom $=2^{\mathrm{n}}=2^{2}=4$ optical isomer
UPTU/ UPSEE-2014
GENERAL ORGANIC CHEMISTRY
232233
Cyclohexane, methylcyclopentane, 1, 3dimethyl cyclobutane and 1, 2, 3-trimethyl cyclopropane are examples of which one of the following?
1 Constitutional isomers
2 Positional isomers
3 Structural isomers
4 Structural as well as positional isomers
Explanation:
,c) Exp: (A,C) : Structural isomers of $\mathrm{C}_{6} \mathrm{H}_{12}$ are. Structural isomer or constitutional isomers are compoundhaving same molecular formula but different structural formula.
The compound which has restricted rotation around carbon-carbon double bond and substituent attached to alkene must be different if it satisfy these condition the molecule exhibit geometrical isomer For the show enantiomerism it must have asymmetric center with non-superimposable mirror image and also it does not place of symmetry. Those molecule exhibit is show both geometrical and enantiomerism In compound (d) it has both restricted rotation as well as a symmetric center
UPTU/ UPSEE-2016
GENERAL ORGANIC CHEMISTRY
232228
A solution of D-glucose in water rotates the plane of polarised light
1 to the left
2 to the right
3 to either side
4 None of these
Explanation:
We know that glucose is optical active compound because it has more than one asymmetric center so it show optical active which rotate the plane polarized light in either leuollelt for dextro direction It is a natural glucose Natural glucose is dextro rotator (Clockwise) and this glucose is known as dextrose. Thus it rotate the plane polarized light to the right in water.
UPTU/ UPSEE-2015
GENERAL ORGANIC CHEMISTRY
232230
A compound contains two dissimilar asymmetric $\mathrm{C}$-atoms. The number of optical isomers is
1 1
2 2
3 4
4 8
Explanation:
A compound have two asymmetric center ie chiral center in which carbon is $\mathrm{sp}^{3}$ hybridised with different subsistent then the Number of optical isomer $=2^{n}$ Where $n$ is chiral center of carbon atom $=2^{\mathrm{n}}=2^{2}=4$ optical isomer
UPTU/ UPSEE-2014
GENERAL ORGANIC CHEMISTRY
232233
Cyclohexane, methylcyclopentane, 1, 3dimethyl cyclobutane and 1, 2, 3-trimethyl cyclopropane are examples of which one of the following?
1 Constitutional isomers
2 Positional isomers
3 Structural isomers
4 Structural as well as positional isomers
Explanation:
,c) Exp: (A,C) : Structural isomers of $\mathrm{C}_{6} \mathrm{H}_{12}$ are. Structural isomer or constitutional isomers are compoundhaving same molecular formula but different structural formula.
The compound which has restricted rotation around carbon-carbon double bond and substituent attached to alkene must be different if it satisfy these condition the molecule exhibit geometrical isomer For the show enantiomerism it must have asymmetric center with non-superimposable mirror image and also it does not place of symmetry. Those molecule exhibit is show both geometrical and enantiomerism In compound (d) it has both restricted rotation as well as a symmetric center
UPTU/ UPSEE-2016
GENERAL ORGANIC CHEMISTRY
232228
A solution of D-glucose in water rotates the plane of polarised light
1 to the left
2 to the right
3 to either side
4 None of these
Explanation:
We know that glucose is optical active compound because it has more than one asymmetric center so it show optical active which rotate the plane polarized light in either leuollelt for dextro direction It is a natural glucose Natural glucose is dextro rotator (Clockwise) and this glucose is known as dextrose. Thus it rotate the plane polarized light to the right in water.
UPTU/ UPSEE-2015
GENERAL ORGANIC CHEMISTRY
232230
A compound contains two dissimilar asymmetric $\mathrm{C}$-atoms. The number of optical isomers is
1 1
2 2
3 4
4 8
Explanation:
A compound have two asymmetric center ie chiral center in which carbon is $\mathrm{sp}^{3}$ hybridised with different subsistent then the Number of optical isomer $=2^{n}$ Where $n$ is chiral center of carbon atom $=2^{\mathrm{n}}=2^{2}=4$ optical isomer
UPTU/ UPSEE-2014
GENERAL ORGANIC CHEMISTRY
232233
Cyclohexane, methylcyclopentane, 1, 3dimethyl cyclobutane and 1, 2, 3-trimethyl cyclopropane are examples of which one of the following?
1 Constitutional isomers
2 Positional isomers
3 Structural isomers
4 Structural as well as positional isomers
Explanation:
,c) Exp: (A,C) : Structural isomers of $\mathrm{C}_{6} \mathrm{H}_{12}$ are. Structural isomer or constitutional isomers are compoundhaving same molecular formula but different structural formula.
The compound which has restricted rotation around carbon-carbon double bond and substituent attached to alkene must be different if it satisfy these condition the molecule exhibit geometrical isomer For the show enantiomerism it must have asymmetric center with non-superimposable mirror image and also it does not place of symmetry. Those molecule exhibit is show both geometrical and enantiomerism In compound (d) it has both restricted rotation as well as a symmetric center
UPTU/ UPSEE-2016
GENERAL ORGANIC CHEMISTRY
232228
A solution of D-glucose in water rotates the plane of polarised light
1 to the left
2 to the right
3 to either side
4 None of these
Explanation:
We know that glucose is optical active compound because it has more than one asymmetric center so it show optical active which rotate the plane polarized light in either leuollelt for dextro direction It is a natural glucose Natural glucose is dextro rotator (Clockwise) and this glucose is known as dextrose. Thus it rotate the plane polarized light to the right in water.
UPTU/ UPSEE-2015
GENERAL ORGANIC CHEMISTRY
232230
A compound contains two dissimilar asymmetric $\mathrm{C}$-atoms. The number of optical isomers is
1 1
2 2
3 4
4 8
Explanation:
A compound have two asymmetric center ie chiral center in which carbon is $\mathrm{sp}^{3}$ hybridised with different subsistent then the Number of optical isomer $=2^{n}$ Where $n$ is chiral center of carbon atom $=2^{\mathrm{n}}=2^{2}=4$ optical isomer
UPTU/ UPSEE-2014
GENERAL ORGANIC CHEMISTRY
232233
Cyclohexane, methylcyclopentane, 1, 3dimethyl cyclobutane and 1, 2, 3-trimethyl cyclopropane are examples of which one of the following?
1 Constitutional isomers
2 Positional isomers
3 Structural isomers
4 Structural as well as positional isomers
Explanation:
,c) Exp: (A,C) : Structural isomers of $\mathrm{C}_{6} \mathrm{H}_{12}$ are. Structural isomer or constitutional isomers are compoundhaving same molecular formula but different structural formula.
