Correct IUPAC name of the compound 

1. 4-(Ethyl methanolyonxy)phenylpropanoate

2. Ethyl 4-propanoyloxybenzenecarboxylate

3. 4-(1-Oxo-2-oxabutyl)phenylpropanoate

4. 1-(1-Oxo-2-oxbutyl)-4-(1-oxopropoxy)benzene

Subtopic:  Nomenclature |
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Correct IUPAC name of the compound  is

(1) 2-Ethyl-3-methylbut-2-ene-1,4-dioic anhydride

(2) 3-Ethyl_2-methylbut-2-enedioic anhydride

(3) 2-Ethyl-3-Methyl-1,4-diketobut-2-enoic anhydride

(4) 2-Ethyl-3-methylcyclopenatanoxy-1,4-dione

Subtopic:  Nomenclature |
 66%
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The IUPAC name of the following compound is

1. 2-(Ethoxycarbonyl)benzoylchloride

2. Ethyl 2-(chlorocarbonyl)benzoate

3. Ethyl 2-(chloromethanoyl)benzoate

4. Methyl 2-(Chlorocarbonyl)benzene carboxylate.

Subtopic:  Nomenclature |
From NCERT
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A hydrocarbon (R) has six membered ring in which there is no unsaturation. Two alkyl groups are atttached to the ring adjacent to each other. One group has 3 carbon atoms with branching at 1st carbon atom of chain and another has 4 carbon atoms. The larger alkyl group has main chain of three carbon atoms of which second carbon is substituted. Correct IUPAC name of compound (R) is

(1) 1-(1-Methylethyl)-2-(1-methylpropyl)cyclohexane

(2) 1-(2-Methylethyl)-2-(1-methylpropyl)cyclohexane

(3) 1-(1-Methylethyl)-2-(2-methylpropyl)cyclohexane

(4) 1-(1-Methylethyl)-2-butylcyclohexane

Subtopic:  Nomenclature |
 61%
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Identify the structure of x,

(1)

(2)

(3)

(4)

Subtopic:  Nucleophile & Electrophile |
 50%
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In which reaction a chiral reactant is giving a chiral product.

(1) (2) (3) (4)

Subtopic:  Stereo Isomers |
 55%
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Which of the following statements is not correct?

1. A compound whose molecule has D configuration will always be dextrorotatory

2. A compound whose molecule has D configuration may be dextrorotatory or levorotatory

3. A compound whose molecule has R configuration may be dextrorotatory or levorotatory

4. A compound whose molecule has L configuration may be dextrorotatory or levorotatory

Subtopic:  Stereo Isomers |
 67%
From NCERT
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Choose the correct statement among the following: 

1.  Inductive effect transfers e from one carbon atom to another.
2.   Inductive effect operates in both σ\p bonds.
3.     Inductive effect creates no charge in the molecule.
4.      Inductive effect creates partial charges and it is distance-dependent.

Subtopic:  Electron Displacement Effects |
 86%
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The correct stability order of following species is :

(1) x > Y > w > z

(2) y > x > w > z

(3) x > w > z > y

(4) z > x > y > w

Subtopic:  Electron Displacement Effects |
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Which of the following does not represent the resonating structure of

1. 
2. 
3. 
4. 

Subtopic:  Electron Displacement Effects |
 54%
From NCERT
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