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6 CAPS 6 Student Copy GOC AnanthGarg&on Trak0EduCompetishun

The document contains a series of chemistry questions targeting JEE Advanced 2023, including single choice, multiple choice, and integer answer type questions related to bond lengths, basic strength, resonance energy, and other chemical properties. Each question is followed by multiple answer options, and an answer key is provided at the end for reference. The questions cover various concepts in organic chemistry, including stability of carbocations, heat of hydrogenation, and resonance structures.

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0% found this document useful (0 votes)
15 views6 pages

6 CAPS 6 Student Copy GOC AnanthGarg&on Trak0EduCompetishun

The document contains a series of chemistry questions targeting JEE Advanced 2023, including single choice, multiple choice, and integer answer type questions related to bond lengths, basic strength, resonance energy, and other chemical properties. Each question is followed by multiple answer options, and an answer key is provided at the end for reference. The questions cover various concepts in organic chemistry, including stability of carbocations, heat of hydrogenation, and resonance structures.

Uploaded by

9ahardik
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 6

CAPS – 6

CHEMISTRY GOC
TARGET : JEE Advanced - 2023

SINGLE CHOICE QUESTIONS


1. Correct order of bond length of p, q , r , x & y given in following compound is
NH NH
Z q
r
x
CH3 – C – NH
– p
CH3 – C – NH2 CH2  NH CH3 y– NH2

(A) y > x > p > q = z > r (B) y > p > x = z > q > r
(C) p > y > x = z > q > r (D) p > y > x > q = z > r

2.

Correct order of basic strength of this compound is


(A) d > b > c > a (B) c > b > a > d (C) c > a > b > d (D) a > d > c > b
3. Compare rotational energy barrier for the indicated bond.

(A) d > c > b > a (B) a > b > c > d (C) c > d > a > b (D) b > a > d > c
4. Compare C–H bond energy.

(A) a > b > c > d > e > f (B) a > d > c > e > b > f
(C) f > e > d > c > b > a (D) f > b > e > c > d > a
5. Which of the following is correct regarding direction of dipole moment?

(A) (B) (C) (D)

6. The correct order at resonance energy in following.

(A) II > I > III (B) III > II > I (C) I > II > III (D) II > III > I
7. Which molecule has least rotational energy barrier for bond indicated by .
(A) CH3  CH  CH  OMe (B) CH3  CH  CH  NO2
 

(C) (D) O2N  CH  CH  NMe2


Page # 1
8. Statement-1 : is more stable carbocation than .

Statement-2 : + I effect of Me2CH– is more than that of Me–

(A) Statement-1 is true, statement-2 is true and statement-2 is correct explanation for statement-1

(B) Statement-1 is true, statement-2 is true and statement-2 is NOT the correct explanation for
statement-1.

(C) Statement-1 is true, statement-2 is false.

(D) Statement-1 is false, statement-2 is true.

9. Which of the alkene will have maximum Heat of hydrogenation

(A) (B)

(C) (D)

MULTIPLE CHOICE QUESTIONS


10. The tautomeric pairs are

(A) Me2C = NOH and Me2CH–N=O (B) CH2=CH–NHCH3 and CH3–CH=N–CH3

(C) and (D) and

11. Which of the given statement is/are not correct?

(A) is less acidic than CH2 = CH – CH2 – CH = CH2.


 
(B) CH3  NMe3 is more acidic than CH3  PMe3

(C) is more acidic than

(D) is less acidic than

12. Which of the following pairs has 1st having more resonance energy than 2nd.

(A) (B)

(C) (D)

Page # 2
13. Select incorrect statement from the following.

(A) is more basic than

(B) is more acidic than

(C) HC  CH is more acidic than NH3

(D) is more stable than Me – C – O–

14. Select the correct statement.

(A) are positional isomers

(B) are functional isomers

(C) have identical resonance energy.

(D) have identical resonance energy.

15. Which of the following is / are correct order for acidic strength.

(A) (B)

(C) (D)

16. Select the correct order among the following:

(A) Order of heat of hydrogenation

(B) Order of heat of combustion

(C) Order of resonance energy

(D) Order of basic strength

Page # 3
Paragraph for question nos. 17 to 19

17. The correct order of acidic strength of underhed H is


(A) III > I > II > IV (B) I > II > IV > III (C) II > I > III > IV (D) I > II > III > IV
18. Total number of chiral centre present in the molecule is
(A) 6 (B) 7 (C) 9 (D) 10
19. The correct order of bond energy of the marked C – H bond homolysis is:
(A) a > b > c > d (B) d > c > b > a (C) c > b > d > a (D) d > c > a > b

INTEGER ANSWER TYPE


20. Find the total number of the position where positive charge can be delocalized by true resonance

(Excluding the given position)


21. Fill 1 in OMR sheet if the reaction is favoured in forward direction and fill 2 in OMR sheet if the reaction
is favoured in backward direction for example if all the reactions are favoured in forward direction fill
1111 as answer, and if only first two are favoured in forward direction fill 1122 in OMR sheet.
(a) Me – C C–H + NaOH  Me – C C–Na + H2O

O
(b) Ph  OH  NaHCO3  Ph O Na  H2 CO3
 
O
(c) Et  COOH  NaNH2  EtCO O Na  NH3
– 
OH OK
(d) + 2 KOH  + 2 H2 O
– 
OH OK
22. (a) Use the following data to answer the question below:

naphthalene
Calculate the resonance energy of naphthalene in kCal/mol.
(b) How many grams of CO2 is released when 84 gm of sodium bicarbonate is treated with excess of
acetic acid.
If answer of part (a) is xy and part (b) is pq then present your answer as xypq in the OMR sheet
(round of your answer to nearest integers).
For example: if Answer of (a) is 12 and (b) is 13 you will fill 1213 in OMR sheet.

Page # 4
23. How many neutral (Benzoid) resonating structures are possible for.

24. Find out total no. of monoionic resonating structures of the following (Including given)

25. Find out total no. of monoionic resonating structures of the following (Including given)

26. Match the Column.


Column I Column II

(A) (P) Group attached to the benzene ring is +M effect showing group

(B) (Q)Group attached to the benzene ring is –M effect showing group

(C) (R) Group attached to the benzene ring is + H showing group.

(D) (S) Group attached to the benzene ring is –I effect showing group

(T) Compound is aromatic


27. Column I Column II
(Compounds) (Magnitude of heat of hydrogenation)

(A) (P) 52.5 Kcal / mole

(B) (Q) 45.9 Kcal / mole

(C) (R) 26.6 Kcal / mole

(D) (S) 30.7 Kcal / mole

Page # 5
Answer Key
1. (B) 2. (B) 3. (A) 4. (B) 5. (B)
6. (C) 7. (D) 8. (D) 9. (B) 10. (AB)
11. (ABD) 12. (BD) 13. (ABD) 14. (BC) 15. (BCD)
16. (BCD) 17. (D) 18. (C) 19. (B) 20. (10)
21. (2212) 22. (5444) 23. (6) 24. (7) 25. (13)
26. (A) R, T (B) P, S, T (C) Q, S, T (D) P,Q,R,S, T
27. (A) S (B) R (C) Q (D) P

Page # 6

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