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Q4:- Determine the type of the carbocation then predict which one has the highest stability: 4 CH₂ (A) (B) CH, CHA (C) CH, (D)

Q4:- Determine the type of the carbocation then predict which one has the highest stability: 4 CH₂ (A) (B) CH, CHA (C) CH, (D)

Organic Chemistry
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter4: Acids And Bases
Section: Chapter Questions
Problem 4.33P: Complete the equation for the reaction between each Lewis acid-base pair. In each equation, label...
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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 CHA (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 CHA (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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