Which of the following best describes the reaction below.0H3O+, heat+ NH3 CH3*H3CNHCH3H3COHThe reaction is incorrect, the amine should form along withe the carboxylatebecause an acid was used.The reaction is incorrect, adding acids to amides forms ketones and amines, notcarboxylic acids.The reaction is incorrect, acids can not break amines into carboxylic acids andamides.The reaction is correct, the protonated amine forms because an acid is used tobreak the amide.

EXPLANATION: 4th option is correct . Mechanism:Step 1: Protonation of amide carbonylWe will…

Answered: Which of the following best describes…

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...

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What steps would be used to synthesize an organic amine? Group of answer choices Ketone + oxidizing agent →carboxylic acid + ammonia →organic amine Alkene + acid → alcohol + ammonia →organic amine Ether + acid →ester + ammonia →organic amine Alkane + acid → alcohol + ammonia →organic amine Carboxylic acid + alcohol →ester + ammonia →organic amine Aldehyde + oxidizing agent →carboxylic acid + ammonia → organic amine
Question 16.
What is true regarding protein backbones? The protein backbone is different for each protein and contains both amine and carboxylic acid functional groups The protein backbone is the same for each protein and contains both amine and carboxylic acid functional groups The protein backbone is different for each protein and contains amide functional groups The protein backbone is the same for each protein and contains amide functional groups
Manage Your Fo Question 19 of 19 Provide the correct systematic name for the compound shown here. N. N-eth yl-N-meth yl butan amine N- 2- 3- N,N- N,N,N- 4- tetra di tri eth hex but prop pent meth amide al an oic acid yl amine Delete MacBook Air 80 000 DII DD F4 F5 F6 F7 F8 F9 %2$
This compound is mescaline, a hallucinogen. CHO CHO T Which of the following statements is true? Select one: O a. O b. O c. O d. Mescaline is an amine. Mescaline contains an alcohol group. Mescaline is a carboxylic acid. Mescaline is an amine and contains an alcohol group.
1. Amines: reactions What are the products of the following reactions? CH,CH,NHCH, + H,O → CHJ pencast Amines and Amides 42,105 views
question 7
QUESTION 3 Which of the following best describes the reaction below. I H₂C NHCH3 H₂O*, heat H₂C OH O The reaction is incorrect, the amine should form along withe the carboxylate because an acid was used. O The reaction is incorrect, acids can not break amines into carboxylic acids and amides. The reaction is correct, the protonated amine forms because an acid is used to break the amide. O The reaction is incorrect, adding acids to amides forms ketones and amines, not carboxylic acids. +NH,CH*
In condensed structural formulas, the amide group in an amide produced from a carboxylic acid and a secondary amine can be written as -CO-NH-. Write the balanced chemical equation for the hydrolysis of N-ethylethanamide with NaOH. CH, CO-NH CH, CH3 + H2O + NAOH Heat CH3-COOH + Na NH,-CH2-CH3 CH3-CO-NH-CH CH3 + HO+ NaOH Heat → CH3-COO H3o'+ Na NH2-CH2-CH3 CH-CO-NH-CH-CH3 + NAOH Heat → CH CO Na + OHNH-CH2-CH3 Heat CH3-CO-NH-CH2-CH3 + NaOH CH3-COO Na" + NH2-CH2-CH3
Fill-in the missing reagents and products for the synthesis of amines.
Draw the structure of the predominant organic product formed in each of the following reactions. Name the College Chemistry II o CHE 132 Test #3 - Carboxylic Acids, Esters, Amines, Amides 1. reactants and the products (organic substances only.) HO aud, b) Cty-çH- NH NaoH CH3-CH,-Ch CHs-CH-CH-ど + LIOH NaOH -0-CH-CHy こいュ-C。 igozi--yitlon HCL う Csてh-N
QUESTION 3 Which of the following best describes the reaction below. 0 QUESTION 4 What is the major organic product of the reaction below? 0 H₂C NHCH, The reaction is incorrect, the amine should form along withe the carboxylate because an acid was used. The reaction is incorrect, acids can not break amines into carboxylic acids and amides. The reaction is correct, the protonated amine forms because an acid is used to break the amide. O The reaction is incorrect, adding acids to amides forms ketones and amines, not carboxylic acids. Br. A CH₂ B Bry CH₂COOH Br -CH₂ с H₂O, heat ? CHB Br l OH D H₂C -CH₂ +NHCH*

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