1
JEE Advanced 2016 Paper 2 Offline
MCQ (Single Correct Answer)
+3
-1

The major product of the following reaction sequence is:

JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 37 English

A
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 37 English Option 1
B
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 37 English Option 2
C
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 37 English Option 3
D
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 37 English Option 4
2
JEE Advanced 2016 Paper 2 Offline
MCQ (Single Correct Answer)
+3
-1

In the following reaction, sequence in aqueous solution, the species X, Y and Z, respectively, are

$${S_2}O_3^{2 - }\buildrel {A{g^ + }} \over \longrightarrow \mathop X\limits_{Clear\,solution} \buildrel {A{g^ + }} \over \longrightarrow \mathop Y\limits_{White\,precipitate} \buildrel {With\,time} \over \longrightarrow \mathop Z\limits_{Black\,precipitate} $$

A
[Ag(S2O3)2]3$$-$$, Ag2S2O3, Ag2S
B
[Ag(S2O3)2]5$$-$$, Ag2SO3, Ag2S
C
[Ag(SO3)2]3$$-$$, Ag2S2O3, Ag
D
[Ag(SO3)3]3$$-$$, Ag2SO4, Ag
3
JEE Advanced 2016 Paper 2 Offline
MCQ (Single Correct Answer)
+3
-1

The qualitative sketches I, II and III given below show the variation of surface tension with molar concentration of three different aqueous solutions of KCl, CH3OH and CH3(CH2)11 OSO$$_3^ - $$ Na+ at room temperature. The correct assignment of the sketches is

JEE Advanced 2016 Paper 2 Offline Chemistry - Solutions Question 7 English

A

I : KCl

II : CH3OH

III : CH3(CH2)11 OSO$$_3^ - $$ Na+

B

I. CH3(CH2)11 OSO$$_3^ - $$ Na+

II. CH3OH

III. KCl

C

I. KCl

II. CH3(CH2)11 OSO$$_3^ - $$ Na+

III. CH3OH

D

I. CH3OH

II. KCl

III. CH3(CH2)11 OSO$$_3^ - $$ Na+

4
JEE Advanced 2016 Paper 2 Offline
MCQ (More than One Correct Answer)
+4
-2

For "invert sugar", the correct statement(s) is(are)

(Given : specific rotations of (+)-sucrose, (+)-maltose, L-($$-$$)-glucose and L-(+)-fructose in aqueous solution are +66$$^\circ$$, +140$$^\circ$$, $$-$$52$$^\circ$$ and +92$$^\circ$$, respectively.)

A
"invert sugar" is prepared by acid catalyzed hydrolysis of maltose.
B
"invert sugar" is an equimolar mixture of D-(+)-glucose and D-($$-$$)-fructose.
C
specific rotation of "invert sugar" is $$-$$20$$^\circ$$.
D
on reaction with Br2 water, "invert sugar" forms saccharic acid as one of the products.
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