1
AIPMT 2010 Mains
MCQ (Single Correct Answer)
+4
-1
Which of the following expressions correctly represents the equivalent conductance at infinite diluation of Al2(SO4)3. Given that $$\mathop \Lambda \limits^ \circ $$Al3+ and $$\mathop \Lambda \limits^ \circ $$so$$_4^{2 - }$$ are the equivalent conductances at infinite dilution of the respective ions?
A
$$2\mathop \Lambda \limits^ \circ $$Al3+   +   $$3\mathop \Lambda \limits^ \circ $$so$$_4^{2 - }$$
B
$$\mathop \Lambda \limits^ \circ $$Al3+   +   $$\mathop \Lambda \limits^ \circ $$so$$_4^{2 - }$$
C
($$\mathop \Lambda \limits^ \circ $$Al3+   +   $$\mathop \Lambda \limits^ \circ $$so$$_4^{2 - }$$) $$ \times $$ 6
D
$${1 \over 3}$$$$\mathop \Lambda \limits^ \circ $$Al3+   +   $${1 \over 2}$$$$\mathop \Lambda \limits^ \circ $$so$$_4^{2 - }$$
2
AIPMT 2010 Mains
MCQ (Single Correct Answer)
+4
-1
Fructose reduces Tollen's reagent due to
A
asymmetric carbons
B
primary alcoholic group
C
secondary alcoholic group
D
enolisation of fructose followed by conversion to aldehyde by base
3
AIPMT 2010 Mains
MCQ (Single Correct Answer)
+4
-1
Which one of the following compounds will be most readily dehydrated?
A
AIPMT 2010 Mains Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 55 English Option 1
B
AIPMT 2010 Mains Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 55 English Option 2
C
AIPMT 2010 Mains Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 55 English Option 3
D
AIPMT 2010 Mains Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 55 English Option 4
4
AIPMT 2010 Mains
MCQ (Single Correct Answer)
+4
-1
Match the compounds given in List I with their characteristic reactions given in List II. Select the correct option.

List I
(Compounds)
List II
(Reactions)
A. CH3(CH2)3NH2 (i) Alkaline hydrolysis
B. CH3C$$ \equiv $$CH (ii) With KOH (alcohol)
and CHCl3 produces
bad smell
C. CH3CH2COOCH3 (iii) Gives white ppt.
with ammoniacal
AgNO3
D. CH3CH(OH)CH3 (iv) With Lucas reagent
cloudiness appears
after 5 minutes
A
A-(ii),  B-(i),  C-(iv),  D-(iii)
B
A-(iii),  B-(ii),  C-(i),  D-(iv)
C
A-(ii),  B-(iii),  C-(i),  D-(iv)
D
A-(iv),  B-(ii),  C-(iii),  D-(i)
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