Connect 1-Semester Online Access for Principles of General, Organic & Biochemistry
2nd Edition
ISBN: 9780077633707
Author: Janice Smith
Publisher: Mcgraw-hill Higher Education (us)
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Question
Chapter 13, Problem 13.80AP
a.
Interpretation Introduction
Interpretation:
Product that forms has to be drawn when
Concept Introduction:
Amide also undergo hydrolysis as like esters. They are much less reactive than the esters. When amide is treated with water in presence of base, the product formed is carboxylate salt and
b.
Interpretation Introduction
Interpretation:
Product that forms has to be drawn when
Concept Introduction:
Refer part “a.”.
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Students have asked these similar questions
VI. What ammonium salt is formed when each amine is treated with HCI? Draw the
structure of the resulting salt.
a.
-NH2
b.
-CH,NHCH3
17-50
Draw the structure of the amine salt produced when
each of the following amines reacts with HCl.
a. CH3-CH,-CH2-NH2
b. CH3-NH-CH3
CH3
c. CH,-CH-CH;-NH, d.[NH-CH;-Ch
-NH-CH-CH
V. Classify each amine as 1', 2 or 3'. Give the IUPAC name for each amine.
CH3
a. CH3CHCH,CH2NHCH3
b.
CH3-C-CH,NH2
ČH3
ČH3
Chapter 13 Solutions
Connect 1-Semester Online Access for Principles of General, Organic & Biochemistry
Ch. 13.1 - Draw out each compound to clearly show what groups...Ch. 13.1 - Prob. 13.2PCh. 13.2 - Prob. 13.3PCh. 13.2 - Give the structure corresponding to each IUPAC...Ch. 13.2 - Prob. 13.5PCh. 13.2 - Give the structure corresponding to each name. a....Ch. 13.3 - Which compound in each pair has the higher boiling...Ch. 13.3 - Rank the following compounds in order of...Ch. 13.4 - Which compounds are -hydroxy acids? tartaric acid...Ch. 13.4 - Prob. 13.10P
Ch. 13.5 - Prob. 13.11PCh. 13.5 - Prob. 13.12PCh. 13.5 - Prob. 13.13PCh. 13.6 - Prob. 13.14PCh. 13.6 - Prob. 13.15PCh. 13.6 - Prob. 13.16PCh. 13.6 - Prob. 13.17PCh. 13.6 - Prob. 13.18PCh. 13.6 - Prob. 13.19PCh. 13.7 - Prob. 13.20PCh. 13.7 - Prob. 13.21PCh. 13.7 - Prob. 13.22PCh. 13.7 - Prob. 13.23PCh. 13.7 - Prob. 13.24PCh. 13.8 - Prob. 13.25PCh. 13.8 - Prob. 13.26PCh. 13.8 - Prob. 13.27PCh. 13.8 - Draw the product formed when each ammonium salt is...Ch. 13.8 - Prob. 13.29PCh. 13.9 - Prob. 13.30PCh. 13.9 - Prob. 13.31PCh. 13.9 - Prob. 13.32PCh. 13.9 - Why is the boiling point of CH3CONH2(221C) higher...Ch. 13.9 - Prob. 13.34PCh. 13.9 - Prob. 13.35PCh. 13.10 - Prob. 13.36PCh. 13 - Prob. 13.37UKCCh. 13 - Prob. 13.38UKCCh. 13 - Prob. 13.39UKCCh. 13 - Prob. 13.40UKCCh. 13 - Prob. 13.41UKCCh. 13 - Prob. 13.42UKCCh. 13 - Prob. 13.43UKCCh. 13 - Prob. 13.44UKCCh. 13 - Prob. 13.45UKCCh. 13 - Prob. 13.46UKCCh. 13 - Prob. 13.47UKCCh. 13 - Prob. 13.48UKCCh. 13 - Prob. 13.49UKCCh. 13 - Prob. 13.50UKCCh. 13 - Prob. 13.51APCh. 13 - Prob. 13.52APCh. 13 - Prob. 13.53APCh. 13 - Draw the structure of a compound of molecular...Ch. 13 - Prob. 13.55APCh. 13 - Prob. 13.56APCh. 13 - Give an acceptable name for each compound.Ch. 13 - Prob. 13.58APCh. 13 - Prob. 13.59APCh. 13 - Prob. 13.60APCh. 13 - Prob. 13.61APCh. 13 - Prob. 13.62APCh. 13 - Prob. 13.63APCh. 13 - Give an acceptable name for each amine or amide....Ch. 13 - Draw the structure corresponding to each name. a....Ch. 13 - Draw the structure corresponding to each name. a....Ch. 13 - Prob. 13.67APCh. 13 - Draw the structure of each amine or ammonium salt....Ch. 13 - Prob. 13.69APCh. 13 - Which compound in each pair is more water soluble?...Ch. 13 - Prob. 13.71APCh. 13 - Prob. 13.72APCh. 13 - Prob. 13.73APCh. 13 - Prob. 13.74APCh. 13 - Prob. 13.75APCh. 13 - Prob. 13.76APCh. 13 - Prob. 13.77APCh. 13 - Prob. 13.78APCh. 13 - Prob. 13.79APCh. 13 - Prob. 13.80APCh. 13 - Prob. 13.81APCh. 13 - Prob. 13.82APCh. 13 - Prob. 13.83APCh. 13 - Prob. 13.84APCh. 13 - Prob. 13.85APCh. 13 - Prob. 13.86APCh. 13 - Prob. 13.87APCh. 13 - Draw the products of each acid-base reaction.Ch. 13 - Prob. 13.89APCh. 13 - Prob. 13.90APCh. 13 - Prob. 13.91APCh. 13 - Prob. 13.92APCh. 13 - Ritalin is the trade name for methylphenidate, a...Ch. 13 - Prob. 13.94APCh. 13 - Prob. 13.95CPCh. 13 - Prob. 13.96CPCh. 13 - Prob. 13.97CPCh. 13 - Prob. 13.98BTCCh. 13 - Prob. 13.99BTCCh. 13 - Prob. 13.100BTC
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Similar questions
- Draw the structure of the amine salt produced when each of the following amines reacts with HCl. 6-50 a. CH3-CH2-CH2-NH2 b. CH3-NH-CH3 CH3 c. CH-CH-CH2-NH2 d. NH-CH-CHarrow_forwardArrange the following amines in increasing boiling point. O₂N. NH₂ NH₂ NH₂ A a. Carrow_forwardAssign a common name to each of the following amines. 17-16 a. CH3-CH-CH3 NH2 b. H2N-CH2-CH,-CH2-CH; c. CH3-CH2-Ņ-CH,-CH3 ČH,-CH3 d. CH3-CH2-CH2–NH-CH-CH3 ČH3arrow_forwardErythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. What functional group Erythronolide B does contain? a. b. H₂CH₂C C. H₂C 1 H₂C 2 3 4 O Amide d. Amine OH Erythronolide B Ketone Aldehyde a CH₂ b C d CH₂ OH JCH₂ 'OH OHarrow_forwardDraw the major product formed by treating each amine with excess CH3I, followed by Ag,0, and then heat. -CH,CHCH3 NH2 а. b. C. H2Narrow_forward7 8 3: H3C H3C. CH₂ CH3 N,N-diethylpropanamine N-ethyl-pentanamine 3-ethylhexanamine 3-propylpentanaminearrow_forward1 32. Chich of the following functional groups on an amide CANNOT hydrogen bond with water? 33. O-C=O NH₂ CH3 O all the above can hydrogen bond with water What are the products of the following hydrolysis reaction. O O= CH₂CH₂C-OH + CH₂NH₂ C CH,CH,C-O + CH,NH* CH,CH,C-NH, + CH, C1 O Ο O CH₂CH₂C-OH + CH3NH₂ O no correct response JUN ty X a CH₂CH₂C-NHCH₂ + H₂O + HCl- a 130 W ? Xarrow_forward2. Methadone, a narcotic analgesic (shown below as the amine), is dispensed as its hydrochloride salt. Explain the use of the salt rather than the amine. Use the structure shown and convert it to the HOLT 24th hydrochloride salt. N-CH3 H3C CHIA peop Methadone GHL aco Hot 40arrow_forwardGive a systematic name for each amide ?arrow_forwardClassify each of the following as a primary, secondary, or tertiary amine: NH-CH3 a. CH,CH,-N-CH,CH; c. CH3 CH3 CH3 b. CH,-C-NH, ČH3 d.arrow_forwardDraw the products formed when each carbonyl compound reacts with the following amines: (1] CH,CH,CH,NH2; [2] (CH3CH2)NH. cOCI 요요 b. .C. CH a. CH3arrow_forwardWhat amide(s) will form each of the following amines on treatment with LIAIH4? CH2NH2 CH2CH3 'N' c. CH3CH,NHC(CH3)3 a. CH,CH,arrow_forwardarrow_back_iosSEE MORE QUESTIONSarrow_forward_ios
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