Isomerism Flashcards

1
Q

How many isomers are there for C4H10, C5H12, C6H14 and C7H16?

A

2, 3, 5 and 9

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2
Q

Chain Isomerism

A

Compounds having the same molecular formula but different selection of principal carbon chain

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3
Q

Position Isomerism

A

Compounds having same molecular formula but different position of the functional group, substituent or multiple bond

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4
Q

Functional Isomerism

A

Compounds having the same molecular formula but different types of functional groups are present

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5
Q

Metamerism

A

Different numbers of carbon atoms present bivalent atom or the functional group present in them

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6
Q

Tautomerism

A

Special case of functional isomerism that are in dynamic equilibrium with each other

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7
Q

Conformers

A

Compounds that are obtained when a molecule is rotated along C-C bond

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8
Q

Staggered and Eclipsed form of ethane

A

Staggered, dihedral angle is 60 degree and eclipse, dihedral angle is 0 degree.

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9
Q

Skew conformers

A

All conformers of C2H6 except for staggered and eclipsed form

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10
Q

Stability of conformers of n-Butane

A

Anti-staggered(180)> Gauche(60)> Partially Eclipsed(120)>Fully eclipsed(0)

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11
Q

Steric and Torosional Strain

A

Repulsion due to bulky group and repulsion between the bond pair

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12
Q

Stability of conformers of cyclo-hexane

A

Chair> Twist Boat> Boat> Half Chair

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13
Q

Stereoisomers

A

Compounds having the same molecular formula, but different orientation of atoms in space

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14
Q

Optical Isomers

A

Compounds having same molecular formula, but they differ from each other based on optical rotation or optical activity

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15
Q

Optical Activity

A

Compounds having same molecular formula, but one of them is dextrorotatory and another one is levorotatory

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16
Q

Conditions for a compound to be chiral atom

A
  1. It must be sp2 hybridise
  2. All four valencies must be satisfied by different atoms on group
17
Q

Conditions for asymmetric and desymmetric molecules

A

POS, COS are absent

18
Q

Condition for opitcal isomerism

A

A compound must be dissymmetric to exhibit optical isomerism
Object and its mirror image should be non-super imposable of each other.

19
Q

Allene

A

Compounds having even number of consecutive double bonds

20
Q

Cumelenes

A

Compounds containing odd number of consecutive double bonds and they do not exhibit optical isomerism

21
Q

Racemic mixture

A

Equi-molar mixture of object and its mirror image

22
Q

Enantiomers

A

Objects and their non-superimposable mirror images are enantiomers to each other.
They have same physical properties.

23
Q

Meso Form

A

Form of optically active substance which will have POS and COS in it. They should be optically inactive.

24
Q

R and S configuration

A

When lowest priority is on vertical line, then clockwise is R form and anti-clockwise is S-form
When lowest priority is on horizontal line, then clockwise is S-form and anti-clockwise is R-form.

25
Q

Total optical isomers if the compound is unsymmetrical having ‘n’ chiral centre

A

2^n

26
Q

Stereogenic Area

A

Part of the molecule which shows stereoisomerism is known as the stereogenic area.

27
Q

D and L form

A

If the principal functional group is on the top and the hydroxyl group w.r.t last chiral is present on the right side of the plane, then it is D-form and if it is present on the left, then it is L-form.

28
Q

E and Z form

A

When the priority due to CIP rule is on the same side, then it is Z form and on the opposite side, then it is E form.

29
Q

If the symmetry is present, then geometrical isomerism is

A

2^n