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Which one of the following pairs represents stereoisomerism?
(d) Pair of optical isomerism and geometrical isomerism are able to exhibit the phenomenon of stereoisomerism because both types of isomers differ only in their orientation in space.
-D-glucose and -D glucose have a specific rotation of +112 and +19 respectively. In aqueous solution the rotation becomes +52. This process is called:
(c) The conversion of -glucose and -glucose is called mutarotation.
Racemic mixture is formed by mixing two:
(d) A pair of d- l-optical isomers, i.e, enantiomer on mixing in equal moles gives racemic mixture.
A compound of molecular formula C7H16 shows optical isomerism, compound will be
Stereoisomers (geometrical or opticals) which are neither superimposable nor mirror image to each other are called:
(d) It is the definition of diastereoisomers.
Diastereomers can be separated by:
(a)
The angle of rotation of plane of polarized light depends upon:
(d) Read optical activity
The process of separation of racemic mixture into d- and l-enantiomers is called:
(b) It is definition of resolution.
Which of the following will exhibit chirality?
(b) 3-methyl hexane contains chiral carbon atom, it exhibits chirality.
HCH3-CH2-C*(CH3)-CH2CH2CH3
Number of tertiary carbon atoms in tertiary butyl alcohol is:
The number of isomers for the aromatic compound of the formula C7H8O is:
Which one of the following is the stable structure of cyclohexatriene?
(d) Benzene has planar structure.
Meso tartaric acid is optically inactive due to the presence of:
The rotation by upper half is internally compensated by the rotation of lower half to produce inactive nature.
The property by virtue of which a compound can turn the plane of polarization of light is known as:
(c) It is the definition of optical activity.
The molecular formula of a saturated compound is C2H4Br2.This formula permits the existence of:
(c) 1,1-dibromoethane and 1,2-dibromoethane.