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37. Which one of the folowing reagents is most suitable for converting of H. H-C- C-C-C into HO, H. H. A) PCL, at 50°C B) SOČI, at room temperature C) conc. HCI at 80°C D) CI, in bright sunlight at 100°C 38 Which of the following is the main organic product when BrCH COBr is treated with cold water? A) HOCH,COBr C) HOCH,COOH B) BRCH,CO,H D) HOCH,CHO 39. Which of the following compounds will react with the product of ils own oxidation to form a sweet smelling liquid? A) butanai B) butan -1-ol C) butan - 2- ol D) butanoic acid

37. Which one of the folowing reagents is most suitable for converting of H. H-C- C-C-C into HO, H. H. A) PCL, at 50°C B) SOČI, at room temperature C) conc. HCI at 80°C D) CI, in bright sunlight at 100°C 38 Which of the following is the main organic product when BrCH COBr is treated with cold water? A) HOCH,COBr C) HOCH,COOH B) BRCH,CO,H D) HOCH,CHO 39. Which of the following compounds will react with the product of ils own oxidation to form a sweet smelling liquid? A) butanai B) butan -1-ol C) butan - 2- ol D) butanoic acid

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Answer Q 37, 38 & 39 showing clearly all working and detailed explanations

35 The product formed when an acythalide reacts with ammonia is? A) an ester C) an amide Questions 42 and 43 os of CHCOOH CH.COCI CH,COOC,H. B) a nitrile D) an amine nitrile solt 36. Give the reagents nece for the 0-C G. p. 1-C 42 Give the reagents and reaction conditions for the conversion of I to Ii A) SOCI, at room temperature B) CI, in U.V light C) HCI(aq) D) FeCl (aq) / heat following conversion CH,CH CH, C-N, E TWO CH CH CH, NH, A) NH, C) NaOH/Br, stion ARIONS s of 8) HOBr. 43. Give the reagents and reaction conditions D) NaOH 37. Which one of the following reagents is for the conversion of II to lHH d of n A) 2CH,CH,OH/H/ heat B), phenoUNaOH(aq) most suitable for converting of ich is C) hexanol/H OH CI-C-C. into ot at D) benzoic acid/H Cures tions st of YOH A) PCL at 50°C B) SOĆI, at room temperature C) conc. HCI at 80°C D) CI, in bright sunlight at 100°C 38. Which of the folowing is the main organic product when BrCH COBr is treated with cold water? A) HOCH COBr C) HOCH COOH chdmystr A) 44 CHCHOHH Y, Y is HC OH A. Methylethanoate B. Ethylpropanoate C. Elhylethanoate D. Ethylmethanoate Choose equired 50 RO S R B) BRCH,CO H 45. Which of the following molecules does not possess enantiomers? A. CH,CH CH CO.H B. CHCIBICHOHCOOH C. CH, - CHCH Br D. CH CIC(CH,)cO.H он D) HOCH CHO 39. Which of the following compounds will react with the product of its own oxidation to form a sweet smelling liquid? A) butanai B) butan -1-ol C) butan - 2- ol D) butanoic acid CHC 46. The systematic name of CH,COCH OH is A. hydroxypropanal B. 3-hydroxypropanal C. 3-hydroxypropanone D. Ketopropanol 40. The compound with formula C,HO, exhibit isomerism. What type of isomerism is exhibitted by this compound? A) stereoisomerism B) functional group isomerism C) structural isomerism D) optical isomerism 41. The boiling points of carbonyls compounds are A) higher than those of carboxylic acid of 47. The saponification of ester of palmitic acid (C„H, COOH) produces A. Soap, glycerol and water B. Glycerol and soap C. Soap and water D. A salt and a soap same number of carbon atoms B) lower than those of carboxylic acid of same number of carbon atoms C) same as those of carboxylic acid of 48. The acid of molecular formula CHO, is isomeric to same number of carbon atoms A A diol D) none of the above. C Anhydride B Ester D. Hydroxyleiher 356
Transcribed Image Text:35 The product formed when an acythalide reacts with ammonia is? A) an ester C) an amide Questions 42 and 43 os of CHCOOH CH.COCI CH,COOC,H. B) a nitrile D) an amine nitrile solt 36. Give the reagents nece for the 0-C G. p. 1-C 42 Give the reagents and reaction conditions for the conversion of I to Ii A) SOCI, at room temperature B) CI, in U.V light C) HCI(aq) D) FeCl (aq) / heat following conversion CH,CH CH, C-N, E TWO CH CH CH, NH, A) NH, C) NaOH/Br, stion ARIONS s of 8) HOBr. 43. Give the reagents and reaction conditions D) NaOH 37. Which one of the following reagents is for the conversion of II to lHH d of n A) 2CH,CH,OH/H/ heat B), phenoUNaOH(aq) most suitable for converting of ich is C) hexanol/H OH CI-C-C. into ot at D) benzoic acid/H Cures tions st of YOH A) PCL at 50°C B) SOĆI, at room temperature C) conc. HCI at 80°C D) CI, in bright sunlight at 100°C 38. Which of the folowing is the main organic product when BrCH COBr is treated with cold water? A) HOCH COBr C) HOCH COOH chdmystr A) 44 CHCHOHH Y, Y is HC OH A. Methylethanoate B. Ethylpropanoate C. Elhylethanoate D. Ethylmethanoate Choose equired 50 RO S R B) BRCH,CO H 45. Which of the following molecules does not possess enantiomers? A. CH,CH CH CO.H B. CHCIBICHOHCOOH C. CH, - CHCH Br D. CH CIC(CH,)cO.H он D) HOCH CHO 39. Which of the following compounds will react with the product of its own oxidation to form a sweet smelling liquid? A) butanai B) butan -1-ol C) butan - 2- ol D) butanoic acid CHC 46. The systematic name of CH,COCH OH is A. hydroxypropanal B. 3-hydroxypropanal C. 3-hydroxypropanone D. Ketopropanol 40. The compound with formula C,HO, exhibit isomerism. What type of isomerism is exhibitted by this compound? A) stereoisomerism B) functional group isomerism C) structural isomerism D) optical isomerism 41. The boiling points of carbonyls compounds are A) higher than those of carboxylic acid of 47. The saponification of ester of palmitic acid (C„H, COOH) produces A. Soap, glycerol and water B. Glycerol and soap C. Soap and water D. A salt and a soap same number of carbon atoms B) lower than those of carboxylic acid of same number of carbon atoms C) same as those of carboxylic acid of 48. The acid of molecular formula CHO, is isomeric to same number of carbon atoms A A diol D) none of the above. C Anhydride B Ester D. Hydroxyleiher 356
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