Isomerism-1 Flashcards

1
Q

what are isomers and what is isomerism

A

Two or more than two compounds having the same molecular formula but different physical/chemical or
both properties are called isomers and the phenomenon is called isomerism.

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2
Q

classification of isomers

A

(i) structural isomerism
- Chain isomers
- Positional isomerism
- Functional isomerism
- Ring chain isomerism
- Metamerism

(ii) Stereoisomerism
- Geometrical Isomerism
- Optical Isomerism

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3
Q

what is chain isomerim

A

when two cpds have same molecular formula, same functional group but different arrangement of carbons in the parent chain .

iso- one methyls carbons surrounding the second carbon

neo- two methyl carbons surrounding the second carbos

min no of carbon for alkane= 4
min no of carbon for alkene= 4
min no of carbon for alkyne=5

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4
Q

what is positional isomerism

A

The compounds which have same molecular formula, same functional group, same parent carbon chain but
different position of functional group or multiple bond or substituents, show position isomerism.
min no of carbon for alkane=6
min no of carbon for alkene=4
min no of carbon for alkyne=4

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5
Q

what is iupac name for triptane

A

2,3,3,- triimethylbutane

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6
Q

what is ringchain isomerism

A

Same molecular formula but different mode of linking (open chain & closed chain) of carbon atoms..
alkene= cycloalkane
alkyne/alkadiene=cycloallkene

ringchain isomers are also functional isomers but priority is fr ring chain isomers

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7
Q

what is functional isomerism

A

Same molecular formula but different functional groups.

  • alcohols, ethers
  • acids, esters
  • aldehydes,ketones
  • nitro and nitrite
  • cyanid and isocyanide
  • primary,secondary,tertiary amines
  • phenolic, alcoholic (benzene ring) cpds

alkyl halides do not show func isomerism

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8
Q

what is metamerism

A

Same molecular formula, same polyvalent Functional group but different alkyl groups attached to polyvalent
Functional group.
Polyvalent Functional group [Which have more than one valency] are :

ether, sulphur
-C-O-
II
O

ketone, acid anhydride

-C-N H -
II
O

-NH-
-N-
I

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9
Q

what are the two types of stereoisomerism

A

(i) Configurational Isomerism
- Geomtircal isomerism
- Optical isomerism

(ii) Conformational Isomerism

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10
Q

what is geometrical isomerism

A

Stereo isomer which cannot interconvert at room temperature due to restricted rotation known as
Geometrical isomerism.

Alkenes ( >C C<), oximes (>C N—) and azo compounds [—N N—] etc., show G. I. due to restricted
rotation about double bond and (ii) cycloalkanes show G. I. due to restricted rotation about single bond in
ring.

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11
Q

what is the condition for geomtetrical isomerism in alkenes

A

Each sp2 hybiridised carbon must have individuallly differentgrps.
If any of the double bonded ccarbons have two same groups bonded with it, then geomtrical isomerism cannot occur

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12
Q

what is cis trans system

A

If same groups are at same side then cis and if same groups are at different side then trans.

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13
Q

what are components of E-Z nomenclatur e

A

E (Entgegen) : When high priority groups are at opposite side.
Z (Zusamman) : When high priority groups are at same side.

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14
Q

give the cip rules

A

they help in determining the high priority and low priority grps

(i) higher the atomic number, more priority
(ii) if two grps have same atomic number then consider the next atom in the chain
(iii) consider miltiple bonds as single bonds

(iv) the grp with higher mass, has more priortiy

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15
Q

Geometrical isomerism in oximes

A

Oximes show G. I. due to restricted rotation about double bond.
l Only those oximes show Geometrical isomerism in which sp2 carbon have two different groups.

syn= if the H and OH are present on the same side

anti= if H and OH are present on opposite sids

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16
Q

what are geometrical isomer in azo cpds

A

.. ..
- N=N-

the nitrogen has a pair of line pair each.
Anti- if lp are present in opp sides

Syn- if lp are present, on same side

17
Q

what is conformational isomerism

A

The different arrangement of atoms in space that result from the free rotation around single bond, are called
conformations. The phenomenon is called conformational isomerism

conformational isomers also c/a rotamers/ conformers

18
Q

what is dihedral or torsional angle

A

the angle b/w the bond of 2 adjacent of 2 atoms.

19
Q

what is staggered conformation
(ii) eclipsed conformation

A

conformations have 60/ 180 as dihderal angle
eclipsed
conformations have 0* ( fully eclipsed) or 120* ( partially eclipsed) as dihedral angle

20
Q

what are skew conformations

A

conformers with any other angle than 0/60/120/180

21
Q

why is the staggered form of butane most stable

A

the methyl grps are placed extremely far away from each other so least repulsions. so most stability

there is least stability in fully eclipsed form due to maximum repuslion between methyl grps.

22
Q

what is the most stable form in ethylene glycol?

A

ethylene glycol= ethane diol
most stable is gauche form due to intramoelcular h bonding in both OH grps

23
Q
A