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(a)
Interpretation:
The IUPAC name of reaction products when ethyl pentanoate undergoes ester hydrolysis under acidic conditions has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as
(a)
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Answer to Problem 16.130EP
The IUPAC names of the products obtained are,
Explanation of Solution
Given name of ester is ethyl pentanoate. The structure of ethyl pentanoate can be given as,
Under acidic conditions, esters undergo hydrolysis resulting in breakage of the carbon‑oxygen single bond that is present between the “acid part” and “alcohol part”. The product that is obtained on ester hydrolysis in acidic conditions is carboxylic acid and an alcohol. The complete reaction and the structure of the product obtained can be written as shown below,
The IUPAC names of the product obtained can be given using
IUPAC names of the products obtained when ethyl pentanoate undergoes hydrolysis under acidic condition are written.
(b)
Interpretation:
The IUPAC name of reaction products when ethyl methanoate undergoes ester hydrolysis under acidic conditions has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as carboxylic acid salt and alcohol.
(b)
![Check Mark](/static/check-mark.png)
Answer to Problem 16.130EP
The structural formula and IUPAC names of the products obtained are,
Explanation of Solution
Given name of ester is ethyl methanoate. The structure of ethyl methanoate can be given as,
Under acidic conditions, esters undergo hydrolysis resulting in breakage of the carbon‑oxygen single bond that is present between the “acid part” and “alcohol part”. The product that is obtained on ester hydrolysis in acidic conditions is carboxylic acid and an alcohol. The complete reaction and the structure of the product obtained can be written as shown below,
The IUPAC names of the product obtained can be given using IUPAC nomenclature of naming the compounds. The IUPAC names and the structure of the product obtained are,
IUPAC names of the products obtained when ethyl methanoate undergoes hydrolysis under acidic condition are written.
(c)
Interpretation:
The IUPAC name of reaction products when isopropyl pentanoate undergoes ester hydrolysis under acidic conditions has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as carboxylic acid salt and alcohol.
(c)
![Check Mark](/static/check-mark.png)
Answer to Problem 16.130EP
The structural formula and IUPAC names of the products obtained are,
Explanation of Solution
Given name of ester is isopropyl pentanoate. The structure of isopropyl pentanoate can be given as,
Under acidic conditions, esters undergo hydrolysis resulting in breakage of the carbon‑oxygen single bond that is present between the “acid part” and “alcohol part”. The product that is obtained on ester hydrolysis in acidic conditions is carboxylic acid and an alcohol. The complete reaction and the structure of the product obtained can be written as shown below,
The IUPAC names of the product obtained can be given using IUPAC nomenclature of naming the compounds. The IUPAC names and the structure of the product obtained are,
IUPAC names of the products obtained when isopropyl pentanoate undergoes hydrolysis under acidic condition are written.
(d)
Interpretation:
The IUPAC name of reaction products when isopropyl methanoate undergoes ester hydrolysis under acidic conditions has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as carboxylic acid salt and alcohol.
(d)
![Check Mark](/static/check-mark.png)
Answer to Problem 16.130EP
The structural formula and IUPAC names of the products obtained are,
Explanation of Solution
Given name of ester is isopropyl methanoate. The structure of isopropyl methanoate can be given as,
Under acidic conditions, esters undergo hydrolysis resulting in breakage of the carbon‑oxygen single bond that is present between the “acid part” and “alcohol part”. The product that is obtained on ester hydrolysis in acidic conditions is carboxylic acid and an alcohol. The complete reaction and the structure of the product obtained can be written as shown below,
The IUPAC names of the product obtained can be given using IUPAC nomenclature of naming the compounds. The IUPAC names and the structure of the product obtained are,
IUPAC names of the products obtained when isopropyl methanoate undergoes hydrolysis under acidic condition are written.
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Chapter 16 Solutions
General, Organic, and Biological Chemistry Seventh Edition
- Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. OH HO CI Br H CI CI Br CI CI Xf x f g Br D OH Br Br H₂N R. IN Ill I -N S OMe D II H CO₂H 1/111 DuckDuckGarrow_forwardThese are synthesis questions. You need to show how the starting material can be converted into the product(s) shown. You may use any reactions we have learned. Show all the reagents you need. Show each molecule synthesized along the way and be sure to pay attention to the regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made along the way, you need to draw both enantiomers and label the mixture as "racemic". All of the carbon atoms of the products must come from the starting material! ? H Harrow_forwardQ5: Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Clearly show stereochemistry by drawing the wedge-and-dashed bonds. Describe the relationship between each pair of the stereoisomers you have drawn.arrow_forward
- Classify each pair of molecules according to whether or not they can participate in hydrogen bonding with one another. Participate in hydrogen bonding CH3COCH3 and CH3COCH2CH3 H2O and (CH3CH2)2CO CH3COCH3 and CH₂ CHO Answer Bank Do not participate in hydrogen bonding CH3CH2OH and HCHO CH3COCH2CH3 and CH3OHarrow_forwardNonearrow_forwardQ4: Comparing (3S,4S)-3,4-dimethylhexane and (3R,4S)-3,4-dimethylhexane, which one is optically active? Briefly explain.arrow_forward
- Nonearrow_forwardNonearrow_forwardGiven the standard enthalpies of formation for the following substances, determine the reaction enthalpy for the following reaction. 4A (g) + 2B (g) → 2C (g) + 7D (g) AHrxn =?kJ Substance AH in kJ/mol A (g) - 20.42 B (g) + 32.18 C (g) - 72.51 D (g) - 17.87arrow_forward
- Determine ASran for Zn(s) + 2HCl(aq) = ZnCl2(aq) + H2(aq) given the following information: Standard Entropy Values of Various Substance Substance So (J/mol • K) 60.9 Zn(s) HCl(aq) 56.5 130.58 H2(g) Zn2+(aq) -106.5 55.10 CI (aq)arrow_forward3) Catalytic hydrogenation of the compound below produced the expected product. However, a byproduct with molecular formula C10H12O is also formed in small quantities. What is the by product?arrow_forwardWhat is the ΔHorxn of the reaction? NaOH(aq) + HCl(aq) → H2O(l) + NaCl(aq) ΔHorxn 1= ________ kJ/molarrow_forward
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