он 1. aqueous H2SO4 -CH3 CH3 2. H2SO4 H20 но 130° a = Proton transfer d = El Elimination f= Sy1 Nucleophilic substitution b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2.

он 1. aqueous H2SO4 -CH3 CH3 2. H2SO4 H20 но 130° a = Proton transfer d = El Elimination f= Sy1 Nucleophilic substitution b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2.

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

CH3 གོན་ནི། ཡོན་ Br₂, H₂C CH₂Br H3C CH3 H₂C CH3 Aldehydes and ketones can be halogenated at their a-position by reaction with Cl₂, Br2, or 12, under acidic conditions. Using Br₂ under acidic conditions, an intermediate enol is formed which adds bromine at the a-position. The reaction stops after the addition of one bromine because the electron-withdrawing halogen decreases the basicity of the carbonyl oxygen, making the protonation less favorable. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions :0: :OH н-он H-OH₂ H₂O H₂C. H3C. CH3 CH3 H3C CH3 H3C CH3 Σα
238) Supply the missing reagents A and B. A Answer: A = Hg(OAc)2, THF, HOC(CH3)3 OC(CH₂) B = NaBH4
Write down the reduction reaction of each molecule using appropriate reagents, listing the following compounds according to their ease of reduction.
Chemistry 11. Propose a mechanism for the following reaction: OH H₂SO4 Heat
Complete the following reaction and write down stepwise reaction mechanism.
9.
Give the major organic product of the following reaction. 1. SOC CH CH₂ OH 2. CH₂OH O CH,CH₂ CH CH,CH₂ a CH,CH₂ OCH, CH OCH₂CH
Write the products of the following aromatic electrophilic substitutions
2. Complete the reactions, no mechanisms. Name each reaction. If no reaction occurs, write NR. a. b. C. d. yox за NaOt-Bu/t-BUOH NaOEVEtOH NaObu/BuOH NaOH, H₂O, heat H+
9.
What alkene is needed to synthesize each 1,2-diol using [1] OsO4 followed by NaHSO3 in H2O; or [2] CH3CO3H followed by −OH in H2O?
pls help with homework thanks