WORKSHEET AH-03
Tor
JEE (MAIN+ADVANCED) 2021
ENTHUSIAST COURSE
rssiing CE
ALKYL HALIDE & ARYL HALIDE
SECTION - |: SINGLE CORRECT TYPE QUESTIONS
1. Consider the following reaction,
a
SOC CH,—CH, — b 1— CH,
In the above reaction which phenomenon will take place:
(A) Inversion (B) Retention (C) Racémisation (D} Isomerisation
OH
CHy—CH, — ba —CH,
2. Ph—C—O—CH, I (P) +
1 J Absto! Abide
CH;
(P) & (Q) respectively is:
H
(A) Ph— t — OH,CH,—Br (B] Ph—CH,=0H, CH,—CH,—Br
CHy
(C) CHy—OH, P= CH CH, (0) CH,—OH, Ph—CH,—CH,—Br
3. CH,(CH,),CH,OH HE, x,
1-butanol
Identify X and the type of mechanism of the reaction?
(A) CH, —CH, CH, &CHp—=Br & $1 (B) CH, —CH, —CH, —CH, —Br & Sy2
(c) ck A 1CHy—Chy & 81 (D) Cr to 1CH,—CHy & S,2
Br Br
4. Consider the féllowing reactions carvied outat the same temperature.
One OO
Which of the following statement is correct about these reaction.
(A) Both the reactions take place at the same rate
(B) The first reaction takes place faster than second reaction
(C} The second reaction takes place faster than first reaction
(D) Both the reactions take place by $1 mechanism
WORKSHEET (AH-03)(CHEMISTRY) 1CHyOH OCH,
The product (A) and (B) ate respectively:
oF oe
CH,Br CH,Br
1 Br Be
° . or oe Ok
CHBr Br HOH tls
SECTION - Il : ONE OR MORE THAN ONE CORRECT TYPE QUESTIONS
H
6. A XK SEY Kand ¥ are
CHy OH
an Br
wx a Vx OY ov OY
CHy OTs CH Br
7. Identify correct steps representing S¢Tinechanisin for the cleavage of ether with HI
R-O-R + HI we Boas®?
H
int
2. | slow
(Ps REQ he ier RI+ HOR (R81)
H
Rw ay? RP Ris 3°) +ROH
(C) R° +1? RI
(p) RP sae
WORKSHEET (AH-03)(CHEMISTRY)agHi (eq)
>———— 8+)
Reaction (I)
8.
Anhya.HI (1 64.)
Reacion ty” (O*F)
Which ofthe following statements isfare correct?
(A) The compounds (B) and (C) are MesC—I and MeOH and reaction (I) proceeds by Sy1 mechanism
(B) The compound (B) and (C) are MeC—OH and Mel and reaction (I) proceeds by $2 mechanism
(C} The compound (E) and (D) are MesC—I and MeOH and reaction (Il) proceeds by Sxl mechanism
(D) The compound (E) and (D) are Me,C—OH and Mel and reaction (ll) proceeds by S,2 mechanism
SECTION - Ill : NUMERICAL ANSWER TYPE QUESTIONS
(SINGLEIDOUBLE, THREE & FOUR DIGITS ANSWER INCLUDING DECIMAL)
9. Most reactive position inthe given reaction,
CH,
a { 4 8 NBS
cH, cH. CH, =CH ———*
10. When trans-2-butene reacts with BrJOCly)X slumber of products are formed. Whereas when trans-2- butene
3
reacts with HBr, Y nuiber of products are formed. Report your answer as [¥ |X ].
oe ek
ANSWER KEY
1B) eee) 3. B) 4. @) 5. (A)
6. (AB) 7. (BC) 8. (AD) % 2 10. (21)
WORKSHEET (AH-03)(CHEMISTRY) 3