(b)CortisoneOHH2CCH-HO-H3COalcohol O carbon-carbon double bond OesterOaldehyde Ocarbon-carbon triple bond OetherO amideOcarboxylate anionOketoneOamineO carboxylic acidO thiol(c) Prostaglandin PGE2COOHНоOHOalcohol O carbon-carbon double bond OesterOaldehyde Ocarbon-carbon triple bond OetherOketoneO amideO carboxylate anionOamineOcarboxylic acidO thiol

b) Cortisone Alcohol Carbon carbon double bond Ketone

(b) Cortisone OH H2C CH O- H3C O alcohol O carbon-carbon double bond ester O aldehyde Ocarbon-carbon triple bond Oether O amide Ocarboxylate anion Oketone O amine O carboxylic acid O thiol (c) Prostaglandin PGE2 СООН но OH Oalcohol O carbon-carbon double bond Oester O aldehyde O carbon-carbon triple bond Oether Oketone O amide Ocarboxylate anion O thiol Oamine O carboxylic acid

(b) Cortisone OH H2C CH O- H3C O alcohol O carbon-carbon double bond ester O aldehyde Ocarbon-carbon triple bond Oether O amide Ocarboxylate anion Oketone O amine O carboxylic acid O thiol (c) Prostaglandin PGE2 СООН но OH Oalcohol O carbon-carbon double bond Oester O aldehyde O carbon-carbon triple bond Oether Oketone O amide Ocarboxylate anion O thiol Oamine O carboxylic acid

Introduction to General, Organic and Biochemistry

11th Edition

ISBN:9781285869759

Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Chapter19: Carboxylic Anhydrides, Esters, And Amides

Section: Chapter Questions

Problem 19.44P

See similar textbooks

Similar questions

16-13 Classify each amino group as primary, secondary, or tertiary and as aliphatic or aromatic. Serotonin (a neurotransmitter) Diphenhydramine (the hydrochloride salt is the antihistamine Benadryl) Lysine (an amino acid)
What is the systematic name for the two compounds? A B CH: ON-ethyl-3-methylpiperidine and 2-methylpyrrolidine N-ethyl-1-methylpiperidine and 2-methylpyrrolidine O 1-ethyl-3-methylpiperdane and 1-amino-2-methylpyrrole O 3-aminoethyl-1methylpiperdane and 2-methyl pyrrole
Which of the following functional groups are present in 3-nitroaniline? nitro O alcohol hydroxyl alkene 3° amine meta-disubstituted phenyl para-disubstituted phenyl ester O ortho-disubstituted phenyl O ether O alkyl O 2° amine O 1° amine ketone O amide O aldehyde
7 8 3: H3C H3C. CH₂ CH3 N,N-diethylpropanamine N-ethyl-pentanamine 3-ethylhexanamine 3-propylpentanamine
CH,CH,COOH Carboxylic Acid SOCI₂ H₂O Acid anhydride CH₂CH₂COO-Na Acid chloride CH,OH Ester CH,CH,NH, Amide
Name the following CH3CH2 CH3CCH2CHCH3 CH3CH2 :N(CH3)2 O 44-Diethyl-N,N-dimethylpentyl-2-amine O 44-Diethyl-N,N-dimethylpentane-2-amine 4-Ethyl-4,N.N-trimethylhexane-2-amine 4-Ethyl-4,N,N-trimethylhexyl-2-amine
What is the name of this compound? CH3 H3C NH2 CH3 O ethylmethylbutylammonium O cthylmethyl-sec-butyl-ammoium ON-ethyl-N-methyl-3-butamine ON-ethyl-N-methyl-2-butanamine Z-
Draw the struetre of the following three isomeic amides with chemical feruula CHNO. Amide #1: (E)-N,N-dimethyl-2-butenamide Amide #2: (7)-N-methyl-3-pentenamide Amide #3: (7)-3-hexenamide C'onsider Z sterenchemistry of alkenes. • Draw one structure per sketcher. Add additional sketchers asing the drop-down memu in the hottom right comer. Sepamte structares with - signs from the drop-down mena. O00. IF ChemDoodle ChemDoodie ChemDoodle just the first one is what I could really use help on Amide #1: (E)-N,N-dimethyl-2-butenamide
Which of the following structures contains a hemiacetal group? OH H₂C, OCH3 O Option A O Option B C6H5-CH O Option C OCH3 OCH3 OH HỌC–C—CH, T OCH3 O Option D
The correct IUPAC name of the compound Br Ho CH-C- CH но- -CH=CH2 NH2 OH CH 2-amino-3-bromo-4-formyl-3-hydroxy-5-oxohept-6-enoic acid 0 2-amino-3-bromo-4-formyl-3-hydroxy-5-oxohept-6-eneoic acid 6-amino-5-bromo-4-formyl-5-hydroxy-3-oxohept-1-enoic acid 1-amino-2-bromo-2-hydroxy-4-oxo-5-hexen-3-al-1-oic acid 0 2-amino-3-bromo-4-formyl-3-hydroxy-5-oxo-1-heptene carboxylic acid
aw the products for the following reactions showing the formation of amides. Name the 5. reactants and the products. CH Nit + Ho- Cat b) CH-CH NH looc Cat. oH -WH looc cat 6. Draw the products when each of the amides undergoes acid hydrolysis. Name the reactants and products. HCL Cty- -NH-C_Cy+ 0 HCL b) C-CH-N-&cnycy +4,0 HCL + H,0 dig
Name the following molecules or draw the line structure from the name: 3,3-dichloropentanal 4-chlorononanoic acid formamide H₂N OH 3,3-dimethyl-2-hexanone tricyclohexylamine N-butylbenzamide Bra O- Br 1-chloro-3-pentanone ethyl 2-methylpropanoate potassium propanoate