Which of the following compounds would be most reactive with water acting as a nucleophile orbase?Select one:O a. 4-bromo-1-penteneO b. 3-bromo-1-penteneOc. 5-bromo-1-penteneO d. 2-bromo-1-penteneArrange the compounds below in order of DECREASING reactivity toward ring nitration.BromobenzeneNitrobenzeneBenzeneToluene

In nucleophilic substitution reaction, carbocation intermediate is formed. 3-bromopent-1-ene is…

Answered: se? ect one: a. 4-bromo-1-pentene b.…

se? ect one: a. 4-bromo-1-pentene b. 3-bromo-1-pentene c. 5-bromo-1-pentene d. 2-bromo-1-pentene ange the compounds below in order of DECREASING reactivi omobenzene || Nitrobenzene Benzene Tolue

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter20: Nucleophilic Substitution Reactions: Competing Nucleophiles

Section: Chapter Questions

Problem 2Q

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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

Which of the following compounds would be most reactive with water acting as a nucleophile or
base?
Select one:
O a. 4-bromo-1-pentene
O b. 3-bromo-1-pentene
Oc. 5-bromo-1-pentene
O d. 2-bromo-1-pentene
Arrange the compounds below in order of DECREASING reactivity toward ring nitration.
Bromobenzene
Nitrobenzene
Benzene
Toluene

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