32
'I \ , A stream of electrons from a heated C Iilament was passed between two charged iJS plates kept at a potential difference V esu. If e and m are charge and mass of an . L ', C J k- G electron, respectively, then the value of h/A (where A is wavelength associated w I with electron wave) is given by : J ?-- I (1) 2meV u (2) JmeV )cd 2. 2-chloro-2-methylpentane on reaction C I J I with sodium methoxide in methanol yields : - CH3 I CH3 I (a) C2H5CH2C - OCH3 I (a) C2H5CH2C - OCH3 I CH3 CH3 (b) C2H5CH2C = CH2 I CH3 (3) (a) and (b) (4) All of these I F/Page 2 SPACE FOR ROUGH WORK / VtT r,ind & %WTF ~a0lM cH30H-(

cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I

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Page 1: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I

'I

\ , A stream of electrons from a heated

C Iilament was passed between two charged

iJS plates kept at a potential difference V esu.

If e and m are charge and mass of an .

L

', CJ

k-G

electron, respectively, then the value of

h/A (where A is wavelength associated w

I with electron wave) is given by :

J?--I

(1) 2meV

u (2) JmeV

)cd 2. 2-chloro-2-methylpentane on reaction C

I

J I

with sodium methoxide in methanol

yields :

-CH3 I

CH3 I

(a) C2H5CH2C-OCH3 I

(a) C2H5CH2C-OCH3 I

CH3 CH3

(b) C2H5CH2C=CH2 I

CH3

(3) (a) and (b)

(4) All of these

I

F/Page 2 SPACE FOR ROUGH WORK / VtT r,ind & %WTF ~ a 0 l M

cH30H-(

Page 2: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I

3. Which of the following compounds is

metallic and ferromagnetic ?

4. Which of the following statements al?oul

low density polythene is FALSE ?

(1) It is a poor conductor of electric-i tv . (I) 4~:fQ?fm$hFm%1I (2) Its synthesis requires dioxygen or ,I

peroxide initiator as a catalyst.

(3) It is used in the manufacturcb oI' (3- (m),--*,Jnft % buckets, dust-bins etc. - 3 n g i ~ M % 1

(4) Its s~mthesis requires high pressurcb, (4) F & T ~ + V T ~ ( T - W * ~ ~ , ? ~ F ~I

5. For a linear plot of log (x/m) versus log p o, 'a;T'4.sfg~HMw m~iTTdta3 in a Freundlich adsorption isothcbrm, bbg (xjm) ilq log p % ihd k$h which of the following statements in ~ ~ ~ f m 3 * * m m ~ * ? correct ? (k and n are constants) (kaiTeTI1lmfj)

(1) l / n appears as the intercept. ( I ) r$.

l / n m * 7 w m % 1 LL\& Only l / n appears as the slope. (2) m l / n v 3 h % w 3 m % 1

(3) log ( l ln) appears as the interccy t, I (3) log (I/n) -%wT~/ s ~ l i f i% I

(4) Both k and 1/11appear in the sloprj

term. I . , . .

F/Page 3 SPACE FOR ROUGH Wow / W & W

Page 3: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I

Wjh 7 e l l W j h M T F l F l a ~ m

carbon monoxide are -393.5 and -393.5 7W -283.5 kJ mol-I $ l TPh

-283.5 kJ mol-I, respectively. The heat *$?&R3ia91 (k jq) i )M&ft : of formation (in 1cJ) of carbon inonoxide

per mole is :

The heats of combustion of carbon and 6. WIT:

4 6-L(1) 676.5 '

The hottest region of Bunsen flame shown

in the figure below is :

region 4

Pi h ; r 4

region 3 ih ; r3 region 2 i h ; r 2

region 1 ih;r1

(1) region 2 I @ W m 2

(3) repon 4

(4) region 1

8. Which of the following is an anionic 8. fi93 3 *llp*f%Z'#Z \b? detergent ?

(1) Sodium lauryl sulphate FllftFI Wk?

(2) Cetyltrirneth yl ammonium bromide

(3) Glyceryl oleate (3) fhFlftV MW (4) Sodium stearate (4) flWsm d~&

F/Page 4 SPACE FOR ROUGH WORK / W BiTd di W

Page 4: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I

I 9, '18 g glucose (C6HI2o6) is added to 18 g -(C6HI2O6)d 178.2 g fi4

178.2 g water. The vapor pressure of m m b l v * M % r n m water (in torr) for this aqueous solution w (torr 4 ) :

is :

10. The distillation technique most suited for

separating glycerol from spent-ly e in the

soap industry is :

(1) Fractional &stillation

(2) Steam distillation 1 (2) -(4)

(3)

Simple distillation

Distillation under reduced pressure

1 (4)

(3)

TI-mwww7

'R9l;m~v-

11. The species in which the N atom is in a

state of sp hybridization is :

(2) NO; Efti *.

kl s-pfq,NO2 ;/i

3 c-.-,)

Page 5: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 6: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 7: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 8: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 9: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 10: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 11: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 12: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 13: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 14: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 15: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 16: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 17: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 18: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 19: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 20: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 21: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 22: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 23: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 24: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 25: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 26: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 27: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 28: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 29: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 30: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 31: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I
Page 32: cd 2. 2-chloro-2-methylpentane on reaction C J I I with sodium methoxide in methanol yields : -CH3 I CH3 I (a) C2H5CH2C-OCH3 I (a) C2H5CH2C-OCH3 I CH3 CH3 (b) C2H5CH2C=CH2 I