What is the main problem with using the reaction below for synthesis of the indicated product? NH₂ CH3CH₂I Select one: O a. need to replace Cl with F for good yields b. repeated alkylation of amine can result O C. cost of alkyl halide is prohibitive O d. amine is not reactive enough with alkyl halides O e. too sterically hindered NH

What is the main problem with using the reaction below for synthesis of the indicated product? NH₂ CH3CH₂I Select one: O a. need to replace Cl with F for good yields b. repeated alkylation of amine can result O C. cost of alkyl halide is prohibitive O d. amine is not reactive enough with alkyl halides O e. too sterically hindered NH

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions

Section: Chapter Questions

Problem 20.47P

See similar textbooks

Similar questions

Place the binders below in descending order of acidity (pi) and justify your choice: CH3CN; (C2H5)2O; PCl3; As(C6H5)3; (C2H5)3N
2-cyanophenol (pka 7.0) is even more acidic than the 4-cyanophenol isomer. Propose an explanation of why it is so.
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.
Show how you would convert propan-1-ol to the following compounds using tosylateintermediates. You may use whatever additional reagents are needed. b) propan-1-amine, CH3CH2CH2NH2
1.answer the following questions A. What is reagent used to convert secondary amine to tertiary amine? choices: NH3,SOCL2,H20 and excess NH3,Methylhalide? B. During azide synthesis what is good leaving group? Choices: N3,N2,H20,NH2
The reaction of a nitrile with an alcohol in the presence of a strong acid forms an N-substituted amide. This reaction, known as the Ritter reaction, doesnot work with primary alcohols. a. Propose a mechanism for the Ritter reaction.b. Why does the Ritter reaction not work with primary alcohols?c. How does the Ritter reaction differ from the acid-catalyzed hydrolysis of a nitrile to form an amide?
Predict the products formed in the given reaction (Pls explain your answer) a) 1-propanal and butanoic acid b) 1-propanol and sodium butanoate c) 1-butanol and propanoic acid d) 1-butanol and sodium propanoate
(a) How will you convert the following :(i) Propanone to Propan-2-ol (ii) Ethanal to 2-hydroxy propanoic acid(iii) Toluene to benzoic acid(b) Give simple chemical test to distinguish between :(i) Pentan-2-one and Pentan-3-one (ii) Ethanal and Propanal
Chemistry Draw the product formed when phenylacetaldehyde (C6H5CH2CHO) is treated with reach reagent: f. (CH3)2CHNH2, mild acid g. (CH3CH2)2NH, mild acid h. CH3CH2OH (excess), H+ i. piperidine, mild acid j. HOCH2CH2OH, H+
Propose a series of reactions to synthesize each molecule below and show the structure of the intermediate compounds formed following each step you propose. Do not give handwriting solution.
1. Why does H2 not give an IR spectrum? 2. Explain why primary amines and unsubstituted amides have two NH stretching absorptions. 3. Why do anhydrides show two carbonyl peaks? 4. HCl is known to give addition reactions to carbon-carbon double bonds. Why is this behavior not observed in this reaction? 5. Predict the structure of the product expected from addition of molecular bromine to maleic acid.
What does the reaction of 4-Chloropentan-2-amine reacted with excess CH3l, Ag2O produce? O Hofmann product only O Zaitsev product only O Both Hofmann and Zaitsev products Equal distribution