Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) is heated with each carboxylic acid. Include allhydrogen atoms.Reaction ARingsMoreErase0 N HCHỊCH,CH,COOH +CH,CH(CH,)NH,Q2Q(CH,),CHCH,COOH +CH,CH(CH,)NH,heatheatSelect Draw/ || |GReaction BSelect DrawCRingsMoreс 0 N HEraseQ2Q

Answered: Image /qna-images/answer/d0a37437-1e99-453a-8e23-ea5240f89c8f.jpg

Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. Reaction A Select Rings More Erase / || || 0 N H CH,CH,CH,COOH +CH,CH(CH,)NH, Q2Q (CH,),CHCH,COOH +CH,CH(CH,)NH, heat heat G Draw Reaction B Select / ||||| Draw C Rings More с 0 N H Erase Q2Q

Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. Reaction A Select Rings More Erase / || || 0 N H CH,CH,CH,COOH +CH,CH(CH,)NH, Q2Q (CH,),CHCH,COOH +CH,CH(CH,)NH, heat heat G Draw Reaction B Select / ||||| Draw C Rings More с 0 N H Erase Q2Q

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter24: Amines And Heterocycles

Section24.1: Naming Amines

Problem 3P

See similar textbooks

Similar questions

based on this video: on Hinsberg Test Tests for Amines - MeitY OLabs (8.5min) https://www.youtube.com/watch?v=j5jgMUWri8U Write the reaction (two-step, in skeletal) of each test amine when tested in the Hinsberg Test.
The Ka1 of ascorbic acid is 7.94 x 10-5. Would you expect ascorbic acid dissolved in blood plasma (pH 7.35–7.45) to exist primarily as ascorbic acid or as ascorbate anion? Explain.
Which of the following bases is strong enough to deprotonate N,Ndimethylacetamide [CH3CON(CH3)2, pKa = 30], so that equilibrium favors the products: (a) NaNH2; (b) NaOH?
Determining if a Base Is Strong Enough to Deprotonate an Acid Which of the following bases is strong enough to deprotonate N,Ndimethylacetamide [CH3CON(CH3)2, pKa = 30], so that equilibrium favors the products:(a)NaNH2; (b) NaOH?
SHOW COMPLETE SOLUTIONS Q3. Which isolate has A260/280 ratio of above 2.0?
How would you use the reaction of an amide with lialh4 as the key step in going from bromomocyclohexane to N;N- dimethylaminomethyl cyclohexane?
Lithium propanoate is the conjugate base of __________. CH3CH2CO2H (CH3)2CH2CH2CO2H CH3CO2H CH3CH2CH2CO2H
Isoleucine, another of the twenty amino acids found in proteins, is metabolized by a pathway that includes the following step. Propose a mechanism.
Given that Kb for ammonia is 1.8 * 10-5 and that for hydroxylamine is 1.1 * 10-8, which is the stronger base?
What species is the conjugated base of HPO42-?
what is the structure of o-methylphenoxide anion and what is its pKa?