ORGANIC CHEMISTRY (LOOSELEAF)
6th Edition
ISBN: 9781260475630
Author: SMITH
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Question
error_outline
This textbook solution is under construction.
Students have asked these similar questions
Which of the following is a tertiary amine?
C)
N-H
CH₂
N-CH₂
H₂C
b)
NH₂
CH₂
CH₂
H₂CH
N
CH,
d) H₂c-c
CH,
C-CH₂
CH
Explain why
CH3 CH2 CH2NH2
is a Brønsted
base.
Its water
solutions
are basic.
All
substances
containing
nitrogen
atoms are
Brønsted
bases.
This
amine is a
proton
donor.
This
amine can
ассеpt a
proton
from a
proton
donor.
Because amines are basic, they can often accept a proton. Draw the protonated structure of n-propylamine.
Knowledge Booster
Similar questions
- What is the meaning of the term tertiary (3) when it is used to classify amines? Draw a structural formula for the one tertiary (3) amine known as Hnigs base (N,N-diisopropylethylamine).arrow_forwardExplain why the boiling point of propanamide, CH3CH2CONH2, is considerably higher than the boiling point of N,Ndimethylformamide, HCON(CH3)2 (213 °C vs. 153 °C), even though both compounds are isomeric amides.arrow_forward6arrow_forward
- The product of this reaction is: O CI secondary amide secondary amine primary amide tertiary amide primary amine + 2NH3arrow_forwardDraw the reactions for the following products (any or all) (include all products).arrow_forwardDraw the structure of the following three isomeric amides with chemical formula C6H11NO. Amide #1: (E)-N,N-dimethyl-2-butenamide Amide #2: (Z)-N-methyl-3-pentenamide Amide #3: (Z)-3-hexenamidearrow_forward
- Which of the following compounds cannot form hydrogen bonds with wate O CH3-CH2-OH 0 1 CH3-C-OH 0 I CH3-C-0-CH3 O CH3-CH2-CH3 0 O) CH3-CH)-NH2 Question 55 Aniline is a(n) O cyclic amine with only single bonds O tertiary aromatic amine O primary aromatic amine O secondary aromatic amine five carbon aminearrow_forwardAmines in aqueous solutions are less reactive than amines in gaseous solutions. Select one: O True O Falsearrow_forwardDraw the structures of the products when each of the following amides undergo hydrolysis with NaOH. You may want to reference (Page) Section 18.6 while completing this problem. ▼ CH3 0 CH,—CH,—CH—C—NH, Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charg www NN [1] Submit Part B Request Answer H 120 EXP CONT + Marvin JS by ChemAxon • & H H 120 EXP CONT C N O S CI Br - PFL O CH₂ CH3 CH3-CH₂-CH₂-C-N-CH₂-CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charg Р H C Z Oarrow_forward
- When cyclohexanone was reacted with an amine A. It the reaction formed an enamine, whichof the following is the most likely identity of amine A?arrow_forwardN-Methylpyrrolidine has a boiling point of 81 °C, and piperidine has a boiling point of 106 °C. Tetrahydropyran has a boiling point of 88 °C, and cyclopentanone has a boiling point of 141 °C. These two isomershave a boiling point difference of 53 °C. Explain why the two oxygen-containing isomers have a much larger boilingpoint difference than the two amine isomersarrow_forwardWhat is the product of the following neutralization reaction between an amine and an acid, as shown below? H CH3—N—CH₂ - CH3 ammonium bromide O ethylmethylamine bromide ethylmethylamine ethylmethylammonium bromide + HBr →arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning