Q2:- Determine whether the following statements are True or False 1----- - Individual resonance structures are imaginary 2------------ Electrons move from acid to base 3------------Lewis acids have vacant P orbital 4---- Resonance forms differ in the placement of their pi bonds or lone pairs MILL L

Chemistry
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Chapter1: Chemical Foundations
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Q2:- Determine whether the following statements are True or False
1----------- Individual resonance structures are imaginary
2-
3-
4-
5-
7-
8-
9-
10-
Electrons move from acid to base
-Lewis acids have vacant P orbital
(A)
Resonance forms differ in the placement of their pi bonds or lone pairs
NH, has higher bond angle than H₂O
carbocation intermediate, in the reaction of ethylene and HBr, form in the first step
All R enantiomers are dextrorotatory
-Organic bases have an atom (such as N or O) with a lone pair of electrons
-In addition reaction, one molecule splits into two
------Nucleophile is an electron rich molecule
Q3:- What is the configuration in the following
H
CH₂
Br
Q4:- Determine the type of the carbocation then predict which one has the highest stability:
(B)
CH₁
CH
(C)
CH,
to
(D)
H₂C
Q5:- Draw the structure of the following
1-sec-butyl-3-ethylcyclohexane 5-methylcyclopenta-1,3-diene
pent-1-en-4-yne
Q6:-Which compound in each of the following pairs will react faster in S$2 reaction with OH?
(a) CH,Br or CH₂1
(b) (CH),CCI or CH₂Cl (c) CH₂CH₂1 in ethanol or in dimethyl sulfoxide
Transcribed Image Text:Q2:- Determine whether the following statements are True or False 1----------- Individual resonance structures are imaginary 2- 3- 4- 5- 7- 8- 9- 10- Electrons move from acid to base -Lewis acids have vacant P orbital (A) Resonance forms differ in the placement of their pi bonds or lone pairs NH, has higher bond angle than H₂O carbocation intermediate, in the reaction of ethylene and HBr, form in the first step All R enantiomers are dextrorotatory -Organic bases have an atom (such as N or O) with a lone pair of electrons -In addition reaction, one molecule splits into two ------Nucleophile is an electron rich molecule Q3:- What is the configuration in the following H CH₂ Br Q4:- Determine the type of the carbocation then predict which one has the highest stability: (B) CH₁ CH (C) CH, to (D) H₂C Q5:- Draw the structure of the following 1-sec-butyl-3-ethylcyclohexane 5-methylcyclopenta-1,3-diene pent-1-en-4-yne Q6:-Which compound in each of the following pairs will react faster in S$2 reaction with OH? (a) CH,Br or CH₂1 (b) (CH),CCI or CH₂Cl (c) CH₂CH₂1 in ethanol or in dimethyl sulfoxide
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