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Which compournd is a carboxylic: acid? CH3CH2COH O B. O C. CH3CHCHCH3 он O D. CHCCH
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
6. Which of the following carbocations would NOT be likely to undergo rearrangement? A) CH3CHCHCH3 CH3 CH3 B) CH3CHOCH3 CH3 CH C) CH3CCH2 CH3 D) CH3 CH3CHCH2 E) CH3 CH3CCHCH2CH3 CH3 7. Which alcohol would initially produce the most stable carbocation when treated with concentrated H2SO4? A) CH3 CH3CCH2 CH3 он CH3 B) CH3CHCHCH3 он CH3 C) CH3CHCH2CH2OH CH3 D) HOCH2 CHCH2CH3 E) CH2 OH CH3CHCH2CH3 Page 4
Which is a stronger acid? OCH3OCH2OH O CH3CH2CH2OH Submit Request Answer Part B Which is a stronger acid? CH3CH, OH O CH3CH2 N Hz Submit Request Answer Part C Which is a stronger acid? O CH3OCH2CH2OH O CH3CH2OCH2OH Submit Request Answer Part D Which is a stronger acid? O O CH3CH2COH o O CH3CCH2OH Submit Request Answer
which contain a carboxylic acid? 5 points Which of the following molecules contains a carboxylic acid? (Mark all that are correct) OH ОН е е во себе не е во него
Describe the chirality of the following carboxylic acid: Describe the chirality of the following carboxylic acid: ОН он он он 02R,4S o25,4R 02R,4R o 25,4S Submit Answer Tries 0/1
Which class of compounds is most oxidized? A. alkanes B. ketones C. alcohols D. carboxylic acid E. aldehydes
7. Which of the following is the strongest acid? B. CI C. D. F A. он он он он 8. Predict the position of equilibrium for the following reaction. 9. Predict the position of equilibrium for the following reaction. CEN +
Br он онно Meo он Match the carboxylic acid structure given above with the proper IUPAC name or an acceptable common name. Structure A Structure B Structure Structure D 1.5-methoxypentanoic acid 2. 3-ethyl-4-methylpentanoic acid 3.7-methylhexanoic acid 4 3,3-dimethylbutanoic acid 3-isopropylpentanoic acid 6 heptanoic acid bromoacetic acid -bromoethanoic acid
он он te Acetyl adenosyl phosphate A sum Table 21.1. nclature rules for carboxylic acid derivatives is given in able 21.1 Nomenclature of Carboxylic Acid Derivatives Functional group Structure Name ending -ic acid (-carboxylic acid) Carboxylic acid -oyl halide (-carbonyl halide) 0 Acid halide anhydride Acid anhydride -amide (-carboxamide Amide -oate (-carboxylate) Ester RT 、NH2 (NHR, NR2) -thioate (-carbothioate) Thioester -oyl phosphate 0 Acyl phosphate 3.) List the functional groups shown in table 21.1 on page 817 in order of...
The reaction of a carboxylic acid with an alcohol in the presence of acid is termed Fischer esterification. Ohau. Choo он + СН,ОН На он, + но The electrophile in this reaction is Compound C functions as in this reaction. a. a base scavenger b. a solvent c. a catalyst d. a neutralizer