Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Textbook Question
Chapter 20.3, Problem 5P
Draw the structure corresponding to each name.
a.
b. isopropyl propanoate
c. acetic formic anhydride
d. N-isobutyl-N-methylbutanamide
e.
f. o-cyanobenzoic acid
g.
h. N-ethylhexanamide
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Draw the structure corresponding to each name.
a. 3,3-dimethylpentanoic acid
b. 4-chloro-3-phenylheptanoic acid
c. (R)-2-chloropropanoic acid
d. m-hydroxybenzoic acid
e. potassium acetate
f. sodium α-bromobutyrate
g. 2, 2-dichloropentanedioic acid
h. 4-isopropyl-2-methyloctanedioic acid
Draw the structure corresponding to each name.a. 5-methylheptanoyl chloride b. isopropyl propanoatec. acetic formic anhydride d. N-isobutyl-N-methylbutanamide e. sec-butyl 2-methylhexanoate f. N-ethylhexanamide
Draw the structure corresponding to each name.
a. 3,3-dimethylpentanoic acid
b. 4-chloro-3-phenylheptanoic acid
c. (2R)-2-chloropropanoic acid
d. B,B-dichloropropionic acid
e. m-hydroxybenzoic acid
f. o-chlorobenzoic acid
i. 2,2-dichloropentanedioic acid
j. 4-isopropyl-2-methyloctanedioic acid
g. potassium acetate
h. sodium a-bromobutyrate
Chapter 20 Solutions
Organic Chemistry (6th Edition)
Ch. 20.1 - Prob. 1PCh. 20.2 - Draw the three possible resonance structures for...Ch. 20.2 - Prob. 3PCh. 20.3 - Give an IUPAC or common name for each compound. a....Ch. 20.3 - Problem 22.5 Draw the structure corresponding to...Ch. 20.4 - Problem 22.6 Explain why the boiling point of is...Ch. 20.7 - Prob. 11PCh. 20.7 - Prob. 12PCh. 20.8 - Prob. 13PCh. 20.9 - Problem 22.16 Draw the products of each reaction.
...
Ch. 20.9 - Prob. 17PCh. 20.9 - Problem 22.18 Draw a stepwise mechanism for the...Ch. 20.9 - Prob. 19PCh. 20.10 - Problem 22.20 Fenofibrate is a...Ch. 20.10 - Problem 22.21 What product is formed when the...Ch. 20 - Prob. 33PCh. 20 - 22.40 Give the IUPAC or common name for each...Ch. 20 - 22.41 Give the structure corresponding to each...Ch. 20 - Prob. 36PCh. 20 - 22.43 Explain why is a stronger acid and a weaker...Ch. 20 - (a) Propose an explanation for the difference in...Ch. 20 - Draw the product formed when phenylacetic acid is...Ch. 20 - Prob. 42PCh. 20 - Prob. 43PCh. 20 - Prob. 44PCh. 20 - Prob. 45PCh. 20 - Prob. 46PCh. 20 - Prob. 47PCh. 20 - Prob. 48PCh. 20 - 22.64 What carboxylic acid and alcohol are needed...Ch. 20 - Problem 22.65 Devise a synthesis of each compound...Ch. 20 - 22.70 What polyester or poly amide can be prepared...Ch. 20 - 22.71 What two monomers are needed to prepare each...
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- Draw the structure corresponding to each name.a. 5-methylheptanoyl chlorideb. isopropyl propanoatec. acetic formic anhydrided. N-isobutyl-N-methylbutanamidee. 3-methylpentanenitrilef. o-cyanobenzoic acidg. sec-butyl 2-methylhexanoateh. N-ethylhexanamidearrow_forwardDraw the structure corresponding to each name.a. 3,3-dimethylpentanoic acidb. 4-chloro-3-phenylheptanoic acidc. (R)-2-chloropropanoic acidd. m-hydroxybenzoic acide. potassium acetatef. sodium a-bromobutyrateg. 2, 2-dichloropentanedioic acidh. 4-isopropyl-2-methyloctanedioic acidarrow_forwardDraw the structure corresponding to each name.a. 3,3-dimethylpentanoic acidb. 4-chloro-3-phenylheptanoic acidc. (R)-2-chloropropanoic acidd. m-hydroxybenzoic acide. potassium acetatef. sodium α-bromobutyrateg. 2,2-dichloropentanedioic acidh. 4-isopropyl-2-methyloctanedioic acidi. 3,3-dimethylpentanenitrile j. 4,5-diethyl-2-isopropylnonanenitrilearrow_forward
- Give the structure corresponding to each name.a. cyclohexyl propanoateb. cyclohexanecarboxamidec. benzoic propanoic anhydrided. 3-methylhexanoyl chloride e. octyl butanoatef. N,N-dibenzylformamidearrow_forwardDraw the structure corresponding to each name. a. 2-hydroxyheptanoic acid b. 4-chlorononanoic acid c. 3,4-dibromobenzoic acid d. lithium propanoate e. 2,2-dibromobutanoic acid f. ethyl 2-methylpropanoatearrow_forwardPlease explain the chosen letter. Benzoic acid reacts with conc. HNO3 and conc.H2SO, to give a. o-nitrobenzoic acid b. p-nitrobenzoic acid c. m-nitrobenzoic acid d. p-dinitrobenzoic acidarrow_forward
- Give the structure corresponding to each name.a. cyclohexyl propanoateb. cyclohexanecarboxamidec. 4-methylheptanenitriled. vinyl acetatee. benzoic propanoic anhydridef. 3-methylhexanoyl chlorideg. octyl butanoateh. N,N-dibenzylformamidearrow_forward6. Draw the structure of the following compounds. a. cyclobutanecarboxylic acid b. 3,3-dimethylpentanedioic acid c. 4-aminopentanoic acid d. 2-methylcyclohexanecarboxylic acid e. m-chlorobenzoic acidarrow_forwardDraw the structure of the ff. aldehydes and ketones. a. 3-chlorobutanal 6. 8,8-dibromo -4-cthylcyclo hexanone C. 2,4-dimetnylpontanone • Draw the structure of the ff. compounds. a. oyclobutanecarboxylic acid b. 3,8-dimcthylpontancdioic acid C. 4-aminopcntanoic acid d. 2-mothylcycloheranecarooxylic acid m- chlorobėnzoic acidarrow_forward
- Cyclopentanone is treated with chlorine (Cl2) in the presence of acid (H*). What product is formed? A. Chlorocyclopentane B. 1-chloro-1-hydroxycyclopentane C. 2-chlorocyclopentanone D. 3-chlorocyclopentanonearrow_forwardWhich base is at the 5’ end of the structure shown? A.) A B.) C C.) G D.) T E.) Uarrow_forwardDraw the organic product(s) formed when CH3CH2CH2OH is treated with each reagent. a.H2SO4 b.NaH c.HCl + ZnCl2 d.HBr e.SOCl2, pyridine f.PBr3 g.TsCl, pyridine h. [1] NaH; [2] CH3CH2Br [1] i.TsCl, pyridine; [2] NaSH j.POCl3, pyridinearrow_forward
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