1 |
The criteria for aromatically is presence of |
Uneaturations
Cyclic structure
Presence of 4nx electrons
Presence of 4n + 2n electrons
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2 |
The denationalization involving C - H sigma bond electrons is known as . |
Conjugation
Hyperconjugation
Mesomerism
Resonance
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3 |
Compounds consisting of two or more interlocked rings are called. |
Inclusion compounds
Cage compounds
Catenanes
Crown other
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4 |
Cyclic polymers of ethylene glycol formed by condensation are called. |
Crown ether
Brown ether
Cryptates
Both A and C
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5 |
The common host compound for the formation of inclusion compound is. |
Urea
Thiourea
Cholic acid
All above
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6 |
The compounds whose formation require a host compound and a guest compound are called. |
Exclusion compounds
Inclusion compounds
Crystal compounds
None of the above
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7 |
Which of the following statements is not correct with respect to applications of H- bonding. |
It explains the usual b.p. and m.p of certain class of compound.
It explains the solubility of certain organic compounds in hydroxylic solvents
It explains the lack of ideal behavior in gases and solutions
It has stonrg influence on the configuration of certain molecules.
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8 |
In hydrogen bonding a hydrogen atom is bonded to which of the highly electronegative atoms. |
N
O
F
N,O,F
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9 |
Which of the following organic molecule is not aromatic. |
Benzene
Naphthalene
Anthracene
Cyclo-octatetraene
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10 |
Which of the following class of compounds follow the criteria of aromatically. |
The compounds must have high degree of unsaturation
they must have the property to undergo addition reactions
They must have the property to undergo substitution reactions
They must have the ability to sustain an induced current in NMR
|
11 |
Which of the following statements in not correct with respect to the important characteristics of aromatic compounds. |
They are usually cyclic compounds
They are resistant to usual addition reactions
They usually undergo substitution reactions
They are less stable
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12 |
Which of the following statements is not correct. with respect to resonance. |
The position of atomic nuclei mus be same
The limiting structures must have same number of paired and unpaired electrons.
The energy of the various limiting structures must contribute equally
All above
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13 |
The decrease in electron density at one position accompanied by a corresponding increase at other position is called. |
Inductive effect
Asymmetric effect
Electromeric effect
Resonance effect
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14 |
Which of the following statement is not correct with respect to electrometric effect. |
It is permanent effect
It is brought into play instantaneously at the demand of attacking reagent
It proceeds a polar addition reaction
The original electronic condition is restored after the removal of tacking regent.
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15 |
To complete transfer of a shared pir of electrons to one of the atoms joined by a double or triple bond at the requirement of an attacking reagent is known as. |
Inductive effect
Resonance effect
Eletromeric effect
Stark effect
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16 |
Which of the following case of acid or base strength is not explained by inductive effect. |
Formic acid> acetic acid
Dimethyl amine > trimethyl amine
Dimethyl amine > methyl amine
Chloroacetic acid > acetic acid
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17 |
Correct order of increasing ______ I effect of groups is |
----- NO2 >-----------CN > ------------COOH > -------------F
--------F > -------------COOH>----------CN>--------NO2
-----F> -------------CN>--------NO2 > COOH<div><br></div>
-------CN > ------------COOH > -----------NO2 >----------F
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18 |
Inductive effect can be used to explain |
Dipole moment of chemical bonds
Strength of acids
Strength of bases
All above
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19 |
Which of the following statement in not correct with respect to inductive effect. |
Bond length decrease with increase in inductive effect.
Inductive effect generates polar character in bonds
Variation in strength of aliphatic acids can be explained
It alone cna explain the basically of triphenylamine
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20 |
An induction of dipole or polarity in non polar bond, and consequent electron shifting along a chain of atoms is known as. |
Inductive effect
Resonance effect
Hyper conjugation
None of the above
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