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![Predict the product and write the mechanism.
CH3-CH=CH-CH2-CH3 + NBS-
hv
CCl4](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7b08925a-d4c7-46f3-b2e5-6bf24735608a%2F6c280b8b-cfcf-4540-8d0f-fba31b509268%2F66pfmeq_processed.jpeg&w=3840&q=75)
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- Treating 2-methylpropene with methanol in the presence of sulfuric acid gives tert-butyl methyl ether. CH3 CH3 H,SO, CH,C=CH, + CH,OH CH,C-OCH, ČH3 Propose a mechanism for the formation of this ether.give the products and give the mechanism for the formation of A and BPropose a mechanism for this reaction and account for its regioselectivity. CH CH3 CH3-C=CH, + ICI CH3C-CH,I Cl
- Give step-by-step mechanism for the following reaction.⑤Draw the products for the following reactions. CH 유 -(CH2) 4-CH=CH-CH2-CH=CH-CH2-CH=CH(CHI)y CH3 CH-O-C(CH2)4-CH=CH-CH2-CH=CH-CH2-CH=CH-CCH2) 4 CH3 CH₂O' CH24-CH=CH-CH2-CH=CH-CH2-CH=CH-(CH)-(H Ⓑ H + CH2-0-C-H214-CH3 CH-O -0---(CH2) 12-CH3 3 H 6H H+ +3NaOH (H2-0-1-CH2-CH=CH-CH2-CH=CH-(CH2)4-CH3Predict the major products formed when 2- methyl-1-butene reacts with: H2O, H+. Show the reaction mechanism of the given alkene reactions
- Please help7. Give a Mechanism for the following reaction; show formal charges and significant intermediates. e CH3CH₂NH2 H3O+ N CH₂CH3 + H₂OReaction of HBr with 2-methylpropene yields 2-bromopropane. What is the structure of the carbocation intermediate formed during the reaction? Show the mechanism of the reaction.
- Bicyclo-2,5-heptadiene can be prepared in two steps from cyclopentadiene and vinyl chloride. Provide a mechanism for each step.Reaction of HBr with 2-methylpropene yields 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction? Show the mechanism of the reaction.For each reaction, give the expected substitution product and predict whether the mechanism will be first order (Sw1) or second order (Sw2): 2-chloro-2-methylbutane + CH,COOH b) isobutyl bromide + NaOMe c) 1-iodo-1-methylcyclohexane + CH,CH;OH
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