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Ans. [3]
Sol. Sm+3 (Yellow)
Due to presence of unpaired e–
Q.2
Ans. [1]
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Sol.
Ans. [1]
Sol. Due to Zeff.
Ans. [3]
Sol.
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Ans. [1]
Sol. Li⊕ having minimum radius so maximum hydration and maximum hydration radii.
Ans. [2]
Sol. B2H6 + O2 → B2O3 Boric anhydride
B2H6 + H2O → H3BO3 Boric acid
Ans. [2]
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Sol.
Ans. [2]
Sol.
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Ans. [1]
Sol.
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Ans. [1]
Sol.
N2⊕ClΘ –HCl
N=N
+ H
OH OH
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Ans. [1]
Sol.
O Cl
O +
O AlCl3
O ⊕ Θ
O AlCl3 COOH
H2O
Cl Cl
O O
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Ans. [1]
Sol.
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Ans. [3]
Sol.
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Ans. [4]
CH3 OH
Sol. CH3–CH–CH–CH2–COOH
5 4 3 2 1
Q.15
Ans. [2]
Sol. Thermal reduction
Reduction by (C) and (CO)
Ans. [1]
Sol. Due to unpaired electron and pairings electrons due to strong ligands.
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Ans. [4]
Sol. Due to +I effect
Ans. [4]
Sol. Ozonalayer is depleted due to CFCS
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Ans. [1]
Sol. No. phenolic group
No. Aldehyde group
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Ans. [2]
Sol.
Q.21
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Ans. [2]
Sol.
Ans. [3]
OH
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Ans. [3]
Sol.
Ans. [4]
Sol. Plastic bags
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Ans. [4]
Sol.
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Ans. [3]
Sol.
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Ans. [1]
Sol.
Θ
O O
C–CH2–Br CH–CH2–Br
NaBH4
MeOH
CH3
O
CH–CH2
Ans. [1]
Sol. Dimer of α-D glucose
Acidic hydrolysis
α-D glucose
Ans. [4]
Sol. n – Butyl amine
CH3–CH2–CH2–CH2–NH2
only unhindered 1º Amines are products of this reaction
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Ans. [2]
Sol.
H Br
O–CH3 OH
CH=CH2 CH=CH2
+H–B2
OH
CH–CH3
Br
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