Aniline reacts with bromine in the absence of a Lewis acid to give monosubstitution products. Draw a resonance form that explains this greater reactivity to electrophilic aromatic substitution, and give a brief explanation. NH2 NH2 NH2 NH2 Br Br2 NaHCO3 Br Br

Aniline reacts with bromine in the absence of a Lewis acid to give monosubstitution products. Draw a resonance form that explains this greater reactivity to electrophilic aromatic substitution, and give a brief explanation. NH2 NH2 NH2 NH2 Br Br2 NaHCO3 Br Br

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

The SN2 reaction of 1-chloropropane with which of the following nucleophiles is a carbon chain-lengthening reaction? Ammonia Potassium hydroxide Sodium cyanide Potassium iodide Sodium chloride
Which one of the following molecules CANNOT undergo a nucleophilic aromatic substitution reaction? o O2N. O,N `NO2 NO2 F NO2 NO2 NO2 NO2 `NO2 NO2 Br
Rank the reactivity of the compounds below toward nucleophilic acyl substitution by writing the compounds' letters in the proper blanks in the box below. `NH CI Br CH3 CH3 A В C E rank compounds for acyl substitution reactivity most least reactive reactive
Which carbon will attack the alkyl halide (methyl iodide) in the major organic product of the following substitution reaction? A A B с D B H₂ с CH3 D 1) LDA, THF 2) CH₂I
How do you write out the reactions (reactants, conditions and products) for the following electrophilic aromatic substitution reactions Bromination of methylbenzoate Nitration of anisole (methoxybenzene) Bromination of anisole (methoxybenzene)
Which of the following compounds is the most reactive in the nucleophilic aromatic substitution reaction with NaOH? O o-nitrochlorobenzene O m-nitrochlorobenzene O 3,5-dinitrochlorobenzene O 2,4-dinitrochlorobenzene O p-nitrochlorobenzene
Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons 1) NaNH2, NH3() NaBr + 2) CHзCH2CH2Br
Ketones and aldehydes react with sodium acetylide (the sodium salt of acetylene) to give alcohols, as shown in the following example: R₁ OH 1. HC=C: Na* + R₂ Rí R2 2. H3O+ HC Draw the structure of the major reaction product when the following compound reacts with sodium acetylide, assuming that the reaction takes preferentially from the Re face of the carbonyl group. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • You do not have to explicitly draw H atoms. •If a group is achiral, do not use wedged or hashed bonds on it. E CH3 H3C