(a)
Interpretation: The product formed by the treatment of given compound with
Concept introduction: Primary and secondary
(b)
Interpretation: The product formed by the treatment of given compound with
Concept introduction: Primary and secondary amines on reaction with
(c)
Interpretation: The product formed by the treatment of given compound with
Concept introduction: Primary and secondary amines on reaction with
(d)
Interpretation: The product formed by the treatment of given compound with
Concept introduction: Primary and secondary amines on reaction with
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Organic Chemistry (6th Edition)
- Answer each question for A and B depicted in the ball-and-stick models.a. What is the IUPAC name for each compound?b. What product is formed when each compound is treated with NaOH?c. Name the products formed in part (b).d. Draw the structure of an isomer that is at least 105 times less acidic than each compound.arrow_forward18. Identify the lactone formed by the following hydroxy carboxylic acid. A. A B. B C. C D. D OH OH & & A) B) C) D)arrow_forwardDraw the product(s) formed when A is treated with each reagent.a. NaBH4, CH3OH b. LiAlH4, then H2O c. Ag2O, NH4OH d. CrO3, H2SO4, H2O e. PCCarrow_forward
- Draw the stepwise mechanism for the following reaction. 1. LDA, THF 2. Brarrow_forwardSafrole is a naturally occurring acetal isolated from sassafras plants. Once used as a common food additive in root beer and other beverages, it is now banned because it is carcinogenic. What compounds are formed when safrole is hydrolyzed with aqueous acid? safrolearrow_forwardDraw the product formed when each compound is treated with two equivalents of CH;CH,CH,CHgMgBr followed by H,0. OCH3 a. b. C. CH;CH2 OCH2CH3arrow_forward
- b. a. C. HO Draw the products of each reaction. COOH COOH + NaOCH3 OH OH H₂SO4 H₂SO4arrow_forward2. How many different ß-hydroxyaldehydes and ß-hydroxyketones, including constitutional isomers and stereoisomers, are formed upon treatment of a mixture of acetone and benzaldehyde with base? a. b. 2 c. 3 d. 4arrow_forwardSelect the carbonyl compound which can form only a single enol via tautomerization. A. B. H C. D.arrow_forward
- the carbonyl donor or precursor in the following reaction is: a. A b. B c. C d. NaOHarrow_forward16.42 Draw the products formed when each compound is treated with CH3CH₂COCI, AICI 3. a. b. C. N Z-Iarrow_forward16.41 Draw the products of each reaction. а. HNO3 H2SO4 'NO2 HO b. AICI3 CI С. H. Br2 FeBr3arrow_forward
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