CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317631
\({\rm{R}}\) and \({\rm{S}}\) pairs of enantiomers differ from one another in
1 optical rotation of polarised light
2 solubility in racemic mixture
3 reaction with racemic mixture
4 none of these.
Explanation:
\({\rm{R}}\) and \({\rm{S}}\) enantiomers differ in optical rotation of polarised light.
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317632
The absolute configuration of the following is
1 \(2 \mathrm{~S}, 3 \mathrm{R}\)
2 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
3 \(2 \mathrm{R}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2013
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317633
Correct configuration of the following is
1 \(2 \mathrm{R}, 3 \mathrm{~S}\)
2 \(2 \mathrm{~S}, 3 \mathrm{R}\)
3 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2005
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317634
Which of the following exhibits stereoisomerism? (i) 1,2-Dichloroethylene (ii) 2-Hydroxypropanoic acid (iii) 1, 1-Dichloroethylene (iv) 2-Methylpropane
1 (i) and (iv)
2 (ii) and (iv)
3 (i) and (ii)
4 (iii) and (iv)
Explanation:
1, 2-Dichloroethylene : It can show cis-and trans-forms. 2-Hydroxypropanoic acid : Due to presence of chiral carbon it can show optical isomerism. 1, 1-Dichloroethylene : It cannot show geometrical isomerism due to presence of similar groups on two double bonded carbon atoms. 2-Methylpropane : It cannot show optical isomerism due to achiral carbon. Hence, (1) and (2) will show stereoisomerism.
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317631
\({\rm{R}}\) and \({\rm{S}}\) pairs of enantiomers differ from one another in
1 optical rotation of polarised light
2 solubility in racemic mixture
3 reaction with racemic mixture
4 none of these.
Explanation:
\({\rm{R}}\) and \({\rm{S}}\) enantiomers differ in optical rotation of polarised light.
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317632
The absolute configuration of the following is
1 \(2 \mathrm{~S}, 3 \mathrm{R}\)
2 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
3 \(2 \mathrm{R}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2013
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317633
Correct configuration of the following is
1 \(2 \mathrm{R}, 3 \mathrm{~S}\)
2 \(2 \mathrm{~S}, 3 \mathrm{R}\)
3 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2005
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317634
Which of the following exhibits stereoisomerism? (i) 1,2-Dichloroethylene (ii) 2-Hydroxypropanoic acid (iii) 1, 1-Dichloroethylene (iv) 2-Methylpropane
1 (i) and (iv)
2 (ii) and (iv)
3 (i) and (ii)
4 (iii) and (iv)
Explanation:
1, 2-Dichloroethylene : It can show cis-and trans-forms. 2-Hydroxypropanoic acid : Due to presence of chiral carbon it can show optical isomerism. 1, 1-Dichloroethylene : It cannot show geometrical isomerism due to presence of similar groups on two double bonded carbon atoms. 2-Methylpropane : It cannot show optical isomerism due to achiral carbon. Hence, (1) and (2) will show stereoisomerism.
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317631
\({\rm{R}}\) and \({\rm{S}}\) pairs of enantiomers differ from one another in
1 optical rotation of polarised light
2 solubility in racemic mixture
3 reaction with racemic mixture
4 none of these.
Explanation:
\({\rm{R}}\) and \({\rm{S}}\) enantiomers differ in optical rotation of polarised light.
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317632
The absolute configuration of the following is
1 \(2 \mathrm{~S}, 3 \mathrm{R}\)
2 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
3 \(2 \mathrm{R}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2013
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317633
Correct configuration of the following is
1 \(2 \mathrm{R}, 3 \mathrm{~S}\)
2 \(2 \mathrm{~S}, 3 \mathrm{R}\)
3 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2005
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317634
Which of the following exhibits stereoisomerism? (i) 1,2-Dichloroethylene (ii) 2-Hydroxypropanoic acid (iii) 1, 1-Dichloroethylene (iv) 2-Methylpropane
1 (i) and (iv)
2 (ii) and (iv)
3 (i) and (ii)
4 (iii) and (iv)
Explanation:
1, 2-Dichloroethylene : It can show cis-and trans-forms. 2-Hydroxypropanoic acid : Due to presence of chiral carbon it can show optical isomerism. 1, 1-Dichloroethylene : It cannot show geometrical isomerism due to presence of similar groups on two double bonded carbon atoms. 2-Methylpropane : It cannot show optical isomerism due to achiral carbon. Hence, (1) and (2) will show stereoisomerism.
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317631
\({\rm{R}}\) and \({\rm{S}}\) pairs of enantiomers differ from one another in
1 optical rotation of polarised light
2 solubility in racemic mixture
3 reaction with racemic mixture
4 none of these.
Explanation:
\({\rm{R}}\) and \({\rm{S}}\) enantiomers differ in optical rotation of polarised light.
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317632
The absolute configuration of the following is
1 \(2 \mathrm{~S}, 3 \mathrm{R}\)
2 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
3 \(2 \mathrm{R}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2013
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317633
Correct configuration of the following is
1 \(2 \mathrm{R}, 3 \mathrm{~S}\)
2 \(2 \mathrm{~S}, 3 \mathrm{R}\)
3 \(2 \mathrm{~S}, 3 \mathrm{~S}\)
4 \(2 \mathrm{R}, 3 \mathrm{R}\)
Explanation:
AIIMS - 2005
CHXI12:ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES
317634
Which of the following exhibits stereoisomerism? (i) 1,2-Dichloroethylene (ii) 2-Hydroxypropanoic acid (iii) 1, 1-Dichloroethylene (iv) 2-Methylpropane
1 (i) and (iv)
2 (ii) and (iv)
3 (i) and (ii)
4 (iii) and (iv)
Explanation:
1, 2-Dichloroethylene : It can show cis-and trans-forms. 2-Hydroxypropanoic acid : Due to presence of chiral carbon it can show optical isomerism. 1, 1-Dichloroethylene : It cannot show geometrical isomerism due to presence of similar groups on two double bonded carbon atoms. 2-Methylpropane : It cannot show optical isomerism due to achiral carbon. Hence, (1) and (2) will show stereoisomerism.
