Q. No.The correct order with respect to –I effect of the substituents is:
(R = alkyl)
1. –NH2 > –OR < –F
2. –NR2 < –OR < –F
3. –NH2 > –OR > –F
4. –NR2 > –OR > –F
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The IUPAC name of the above mentioned compound is-
1. 3-Ket-2-methylhex-4-enal
2. 5-Formylhex-2-en-3-one
3. 5-Methyl-4-oxohex-2-en-5-al
4. 3-Keto-2-methylhex-4-enal
With respect to the conformers of ethane, which of the following statements is true?
(1) Bond angle remains same but bond length changes
(2) Bond angle changes but bond length remains same
(3) Both bond angle and bond length change
(4) Both bond angles and bond length remain same
The correct order of acidity among the following is:
1. CH2=CH2 >CH≡CH > CH3C≡CH > CH3-CH3
2. CH≡CH > CH3-C≡CH > CH2=CH2 >CH3-CH3
3. CH≡CH > CH2=CH2 > CH3-C≡CH > CH3-CH3
4. CH3-CH3 > CH2=CH2 > CH3-C≡CH > CH≡CH
The most suitable method used for the separation of 1:1 mixture of ortho and para-nitrophenols is:
| 1. | Chromatography | 2. | Crystallization |
| 3. | Steam distillation | 4. | Sublimation |
The IUPAC name of the compound 
1. 5-formylhex-2-en-3-one
2. 5-methyl-4-2-en-5-el
3. 3-keto-2-methylhex-5-enal
4. 3-keto-2-methylhex-4-enal
The correct statement regarding electrophile is :
| 1. | Electrophile is a negatively charged species and can form a bond by accepting a pair of electrons from another electrophile |
| 2. | Electrophiles are generally neutral species and can form a bond by accepting a pair of electrons from a nucleophile |
| 3. | Electrophiles can be either neutral or positively charged species and can form a bond accepting a pair of electrons from a nucleophile |
| 4. | Electrophile is a negatively charged species and can form a bond by accepting a pair of electrons from a nucleophile |
Which among the given molecules can exhibit tautomerisrn?
1. III Only
2. Both I and III
3. Both Iand II
4. Both II and III
The correct order of strengths of the carboxylic acids :-
(a) I>II>III
(b) II>III>I
(c) III>II>I
(d) lI>I>IlI
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