The IUPAC name of the above-mentioned compound is - 

1. (N-Bromo)-3-methyl-2-oxobutanamide

2. (N-Bromo)-2-oxo-4-methylbutanamide

3. (N-Bromo)-1,2-dioxo-3-methylbutanamine carboxamide

4. (N-Bromo)-1-oxo-2-methylpropane

Subtopic:  Nomenclature |
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Which of the following σ-bonds participate in hyperconjugation?

1. I and II 2. I and V
3. II and IV 4. III and IV
Subtopic:  Electron Displacement Effects |
 76%
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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 |
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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 |
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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 |
 62%
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Identify the structure of x,

(1)

(2)

(3)

(4)

Subtopic:  Nucleophile & Electrophile |
 51%
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In which reaction a chiral reactant is giving a chiral product.

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

Subtopic:  Stereo Isomers |
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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 |
 69%
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Which of the following statements about the inductive effect is correct?

1.  The inductive effect transfers electrons from one carbon atom to another.
2.   The inductive effect operates in both \(\sigma\)- and \(\pi\)-bonds.
3.     The inductive effect does not create any charge in the molecule.
4.      The inductive effect creates partial charges and is distance-dependent.

Subtopic:  Electron Displacement Effects |
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