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

The major product of the following reaction sequence is:

JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 44 English

A
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 44 English Option 1
B
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 44 English Option 2
C
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 44 English Option 3
D
JEE Advanced 2016 Paper 2 Offline Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 44 English Option 4
2
JEE Advanced 2016 Paper 2 Offline
MCQ (Single Correct Answer)
+3
-1
Change Language

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
Change Language

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 8 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
Change Language

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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