a) NaBH4 and H3O+
Interpretation:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated first with NaBH4 and then with H3O+ are to be given.
Concept introduction:
NaBH4, either in water or in alcohol reduce
To give:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated first with NaBH4 and then with H3O+.
Answer to Problem 58AP
The product produced when 1) phenylacetaldehyde is treated first with NaBH4 and then with H3O+ is 2-phenylethanol.
The product produced when acetophenone is treated first with NaBH4 and then with H3O+ is 1-phenylethanol.
Explanation of Solution
Phenylacetaldehyde, being an aldehyde is reduced by NaBH4 to a primary alcohol, 2-phenylethanol.
Acetophenone, being a ketone is reduced by NaBH4 to a secondary alcohol, 1-phenylethanol.
The product produced when 1) phenylacetaldehyde is treated first with NaBH4 and then with H3O+ is 2-phenylethanol.
The product produced when acetophenone is treated first with NaBH4 and then with H3O+ is 1-phenylethanol.
b) Dess-Martin reagent
Interpretation:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with Dess-Martin reagent are to be given.
Concept introduction:
Aldehydes and ketones are not oxidized by Dess-Martin reagent.
To give:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with Dess-Martin reagent.
Answer to Problem 58AP
Phenylacetaldehyde does not react with Dess-Martin reagent.
Acetophenone does not react with Dess-Martin reagent.
Explanation of Solution
Aldehydes and ketones are not oxidized by Dess-Martin reagent.
Phenylacetaldehyde does not react with Dess-Martin reagent.
Acetophenone does not react with Dess-Martin reagent.
c) NH2OH, HCl catalyst
Interpretation:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with NH2OH in the presence of HCl catalyst are to be given.
Concept introduction:
Aldehydes and ketones react with hydroxyl amne in the presence of an acid catalyst to yield aloximes and ketoximes respectively.
To give:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with NH2OH in the presence of HCl catalyst.
Answer to Problem 58AP
The product produced when phenylacetaldehyde is treated with NH2OH in the presence of HCl catalyst is
The product produced when acetophenone is treated with NH2OH in the presence of HCl catalyst is
Explanation of Solution
phenylacetaldehyde reacts with NH2OH in the presence of HCl catalystto yield phenylacetaldoxime.
Acetophenone reacts with NH2OH in the presence of HCl catalyst to give acetophenoneoxime.
The product produced when phenylacetaldehyde is treated with NH2OH in the presence of HCl catalyst is
The product produced when acetophenone is treated with NH2OH in the presence of HCl catalyst is
d) CH3MgBr and H3O+
Interpretation:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated first with CH3MgBr and then with H3O+ are to be given.
Concept introduction:
On treatment with Grignard reagents followed by acidification, aldehydes other than formaldehyde yield secondary alcohols and ketones give tertiary alcohols.
To give:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated first with CH3MgBr and then with H3O+.
Answer to Problem 58AP
The product produced when phenylacetaldehyde is treated first with CH3MgBr and then with H3O+ is
The products produced when acetophenone is treated first with CH3MgBr and then with H3O+ is
Explanation of Solution
When phenylacetaldehyde is treated first with CH3MgBr and then with H3O+ the product produced is 1-phenyl-2-propanol, a secondary alcohol.
When acetophenone is treated first with CH3MgBr and then with H3O+ the product produced is 2-phenyl-2-propanol, a tertiary alcohol.
The product produced when phenylacetaldehyde is treated first with CH3MgBr and then with H3O+ is
The products produced when acetophenone is treated first with CH3MgBr and then with H3O+ is
e) CH3OH, HCl catalyst
Interpretation:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with two equivalents of CH3OH in the presence of HCl catalyst are to be given.
Concept introduction:
Aldehydes react reversibley with two equivalents of an alcohol in the presence of an acid catalyst to yield acetals and ketones react to give ketals.
To give:
The product produced when phenylacetaldehyde is treated with two equivalents of CH3OH in the presence of HCl catalyst.
Answer to Problem 58AP
The product produced when phenylacetaldehyde is treated with two equivalents of CH3OH in the presence of HCl catalyst is
The product produced when acetophenone is treated with two equivalents of CH3OH in the presence of HCl catalyst is
Explanation of Solution
Phenylacetaldehyde reacts with two equivalents of CH3OH in the presence of HCl catalyst to yield an acetal.
Acetophenone reacts with two equivalents of CH3OH in the presence of HCl catalyst to yield a ketal.
The product produced when phenylacetaldehyde is treated with two equivalents of CH3OH in the presence of HCl catalyst is
The product produced when acetophenone is treated with two equivalents of CH3OH in the presence of HCl catalyst is
f) NH2NH2, KOH
Interpretation:
The product produced when 1) phenylacetaldehyde and 2) acetophenone are treated with NH2NH2 in the presence of KOH are to be given.
Concept introduction:
The aldehydes and ketones undergo Wolff-Kishner reduction to yield
To give:
The product produced when 1) phenylacetaldehyde and 2) acetophenone are treated first with NH2NH2 and KOH.
Answer to Problem 58AP
The product produced when phenylacetaldehyde is treated with NH2NH2 and KOH is
The product produced when acetophenone is treated with NH2NH2 and KOH is
Explanation of Solution
Phenylacetaldehyde is reduced by NH2NH2 and KOH to ethylbenzene.
Acetophenone also is reduced by NH2NH2 and KOH to ethylbenzene.
The product produced when phenylacetaldehyde is treated with NH2NH2 and KOH is
The product produced when acetophenone is treated with NH2NH2 and KOH is
g) (C6H5)3P=CH2
Interpretation:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with (C6H5)3P=CH2 are to be given.
Concept introduction:
The reaction given is Wittig reaction. Aldehydes and ketones are converted into
To give:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with (C6H5)3P=CH2.
Answer to Problem 58AP
The product produced when phenylacetaldehyde is treated with (C6H5)3P=CH2 is
The product produced when acetophenone are treated with (C6H5)3P=CH2 is
Explanation of Solution
Phenylacetaldehyde reacts with with (C6H5)3P=CH2 to yield 3-phenylpropene.
Acetophenone reacts with with (C6H5)3P=CH2 to yield 2-phenylpropene.
The product produced when phenylacetaldehyde is treated with (C6H5)3P=CH2 is
The product produced when acetophenone are treated with (C6H5)3P=CH2 is
h) HCN, KCN
Interpretation:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated with HCN, KCN are to be given.
Concept introduction:
Aldehydes and ketones undergo nucleophilic addition reaction.
To give:
The products produced when 1) phenylacetaldehyde and 2) acetophenone are treated first with HCN, KCN to yield their cyanohydrins.
Answer to Problem 58AP
The product produced when phenylacetaldehyde is treated with HCN, KCN is
The products produced when acetophenone is treated with HCN, KCN is
Explanation of Solution
When phenylacetaldehyde is treated with HCN, KCN, it gives phenylacetaldehydecyanohydrin.
When acetophenone is treated with HCN, KCN, it gives acetophenonecyanohydrin.
The product produced when phenylacetaldehyde is treated with HCN, KCN is
The products produced when acetophenone is treated with HCN, KCN is
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Chapter 11 Solutions
EP ORGANIC CHEMISTRY,24 MONTH-OWLV2
- Calculate the total amount of heat transferred as 50 g of Water -10°C. Calculate the total amount of heat transferred as 25 g of water is heated from 50°C to 100°C as a gas. \table[[Specific heat H₂O(g), 2.00°C Η 2 g 5. Calculate the total amount of heat transferred as 50 g of wat Specific heat H₂O (g) 2.00 J/g°C -10 °C. 4.18 J/g°C 2.11 J/g°C 2260 J/g 334 J/g Specific heat H₂O (1) Specific heat H₂O (s) Heat of vaporization Heat of fusion Melting point 6. Calculate the total amount of heat transferred as 25 g of water is heated from 50 °C to 100 °C as a gas. Boiling point 100 °C 0°Carrow_forwardWrite formulas for ionic compounds composed of the following ions. Use units as a guide to your solutions. 24. sodium and nitrate 25. calcium and chlorate 26. aluminum and carbonate 27. CHALLENGE Write the formula for an ionic compound formed by ions from a group 2 element and polyatomic ions composed of only carbon and oxygen.show work step by steparrow_forwardADDITIONAL PRACTICE PRACTICE Problems Write formulas for ionic compounds composed of the following ions. Use units as a guide to your solutions. 24. sodium and nitrate 25. calcium and chlorate 26. aluminum and carbonate 27. CHALLENGE Write the formula for an ionic compound formed by ions from a group 2 element and polyatomic ions composed of only carbon and oxygen. ounds 1998arrow_forward
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