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Xicbse Che Asst 1 Ans
Xicbse Che Asst 1 Ans
Solution :
Cl
1
In the trans form the dipole moments cancels
2
out. So net dipole moment is zero
3 6. 1) R
Br
Solution :
3-bromo-1-chloro cyclohex-1-ene
2. 2) sec-butyl bromide
Solution :
Br
|*
CH 3 − CH − CH 2 − CH 3
R – form
Sec-butyl bromide has one chiral carbon,
7. 1) A-iv, B-ii, C-i, D-iii
hence it is optically active
Solution :
3. 3) CH3 – F < CH3 – Cl < CH3 – Br < CH3 – I
(dipole moment) i) Boiling point α Molecular weight
Solution : 1
ii) Boiling point α
No.of branches
The correct dipole moment order of methyl
halides is Correct boiling point order is
CH3 – Cl > CH3 – F > CH3 –B r > CH3 – I
> > Br > CH3 – Br
4. 4) 1, 5-dibromo-3, 4-diethyl hexane
Solution : (104oC) (92oC) (73.3oC) (38.4oC)
8. 1) Both (A) and (R) are true and the (R) is a
correct explanation of the (A)
Solution :
In vinyl halide C – X bond is formed by sp2-p
overlap. Due to lone pair and π-bond
conjugation C – X bond has partial double
bond nature. Hence it is shorter than C – X
1, 5-dibromo-3, 4-diethyl hexane
bond in alkyl halides.
5. 3) sp3 – p sp2 – p
CH3 – CH2 – X CH2 = CH – X
Solution :
2
9. 3) II, III 13. 4) 7
Solution : Solution :
CH 3
| + Cl2
I) CH 3 − CH − CH 2 − Br
Cl Cl
Isobutyl bromide (1o) *
I *
| Cl (d & l)
II) CH 3 − CH − CH 2 − CH 3 (d & l)
2-iodobutane (2o) Cl
CH 3 Cl
|
III) CH 3 − CH − F
Isopropyl fluoride (2o) 14. 1)
CH 3
| Solution :
IV) CH 3 − C − CH 2 − Cl
| Alkyl halides are more reactive than vinyl and
CH 3 aryl halides towards nucleophilic substitution
Neopentyl chloride (1o) reactions
Br 15. 2) 1 : 1
Solution :
10. 3) 3C2H5OH + PCl3 → 3C2H5Cl + H3PO3
1 mol
Solution : C2H5OH + PCl5 → C2H5Cl + POCl3 + HCl
1 mol
COOH