
(a)
Interpretation:
The product which is formed by the reaction of
Concept introduction:
The curved-arrow notation is used to show the transfer of electrons from one atom to another. The curved arrow has two barbs (head and tail) which represent the direction of electron flow.

Answer to Problem 20.31AP
The curved arrow notation and product for the reaction of
Explanation of Solution
The treatment of sodium methoxide with a
In the first step, the electron pairs of oxygen present in methoxide ion attacks the acyl carbon atom of acetic acid and bonding pair of electrons present in the pi bond of acyl group shifts towards oxygen atom simultaneously. Due this an intermediate is formed as shown below.
Figure 1
In the second step, the regeneration of the acyl group takes place by the movement of electron pair of negative charged oxygen atom and also the removal of hydroxide ion takes place from the intermediate simultaneously. Hydroxide ion gets removed by grabbing the electron pair of
Figure 2
Therefore, methyl acetate is desired product formed by the reaction of
The curved arrow notation and product for the reaction of
(b)
Interpretation:
The product which is formed by the reaction of
Concept introduction:
The curved-arrow notation is used to show the transfer of electrons from one atom to another. The curved arrow has two barbs (head and tail) which represent the direction of electron flow.

Answer to Problem 20.31AP
The curved arrow notation and product for the reaction of of acetic acid are shown below.
Explanation of Solution
The treatment of a base like
Figure 3
Therefore, cesium acetate is desired product formed by the reaction of of
The curved arrow notation and product for the reaction of
(c)
Interpretation:
The product which is formed by the reaction of of acetic acid and the corresponding curved-arrow notation are to be stated.
Concept introduction:
The curved-arrow notation is used to show the transfer of electrons from one atom to another. The curved arrow has two barbs (head and tail) which represent the direction of electron flow.

Answer to Problem 20.31AP
The curved arrow notation and product for the reaction of
Explanation of Solution
The treatment of Grignard reagent with a carboxylic acid results into a nucleophilic substitution reaction. The steps for the formation of the product of the reaction between
In the first step, the bonding electron pairs of
Figure 4
In the second step, the regeneration of the acyl group takes place by the movement of electron pair of negative charged oxygen atom and also the removal of hydroxide ion takes place from the intermediate simultaneously. Hydroxide ion gets removed by grabbing the electron pair of
Figure 5
Therefore, of
The curved arrow notation and product for the reaction of
(d)
Interpretation:
The product which is formed by the reaction of
Concept introduction:
The curved-arrow notation is used to show the transfer of electrons from one atom to another. The curved arrow has two barbs (head and tail) which represent the direction of electron flow.

Answer to Problem 20.31AP
The curved arrow notation and product for the reaction of
Explanation of Solution
The treatment of a base like
Figure 6
Therefore, lithium acetate is desired product formed by the reaction of
The curved arrow notation and product for the reaction of
(e)
Interpretation:
The product which is formed by the reaction of
Concept introduction:
The curved-arrow notation is used to show the transfer of electrons from one atom to another. The curved arrow has two barbs (head and tail) which represent the direction of electron flow.

Answer to Problem 20.31AP
The curved arrow notation and product for the reaction of
Explanation of Solution
The treatment of ammonia with a carboxylic acid results into a nucleophilic acyl substitution reaction. The steps for the formation of the product of the reaction between
In the first step, the lone of pair of electrons of
Figure 7
In the second step, electron pairs of oxygen in
Figure 8
In the third step, the regeneration of the acyl group takes place by the movement of electron pair of negative charged oxygen atom and also the removal of hydroxide ion takes place from the intermediate simultaneously. Hydroxide ion gets removed by grabbing the electron pair of
Figure 9
Therefore,
The curved arrow notation and product for the reaction of
(f)
Interpretation:
The product which is formed by the reaction of
Concept introduction:
The curved-arrow notation is used to show the transfer of electrons from one atom to another. The curved arrow has two barbs (head and tail) which represent the direction of electron flow.

Answer to Problem 20.31AP
The curved arrow notation and product for the reaction of
Explanation of Solution
The treatment of a base like
Figure 10
Therefore, sodium acetate is desired product formed by the reaction of
The curved arrow notation and product for the reaction of
(g)
Interpretation:
The product which is formed by the reaction of
Concept introduction:
The curved-arrow notation is used to show the transfer of electrons from one atom to another. The curved arrow has two barbs (head and tail) which represent the direction of electron flow.

Answer to Problem 20.31AP
The curved arrow notation and product for the reaction of
Explanation of Solution
The given compound is shown below.
Figure 11
The given compound is sodium hydrogencarbonate. The treatment of a base like sodium hydrogencarbonate with acetic acid produces a salt known as sodium acetate. In the first step of the reaction between
Figure 12
Therefore, sodium acetate is desired product formed by the reaction of
The curved arrow notation and product for the reaction of
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Chapter 20 Solutions
Organic Chemistry Study Guide and Solutions
- You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products: xi 1. ☑ 2. H₂O хе i Draw the missing reagent X you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. There is no reagent that will make this synthesis work without complications. : ☐ S ☐arrow_forwardPredict the major products of this organic reaction: H OH 1. LiAlH4 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. G C टेarrow_forwardFor each reaction below, decide if the first stable organic product that forms in solution will create a new C-C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 CI MgCl ? Will the first product that forms in this reaction create a new CC bond? Yes No MgBr ? Will the first product that forms in this reaction create a new CC bond? Yes No G टेarrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. དྲ。 ✗MgBr ? O CI Will the first product that forms in this reaction create a new C-C bond? Yes No • ? Will the first product that forms in this reaction create a new CC bond? Yes No × : ☐ Xarrow_forwardPredict the major products of this organic reaction: OH NaBH4 H ? CH3OH Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. ☐ : Sarrow_forwardPredict the major products of this organic reaction: 1. LIAIHA 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. X : ☐arrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new C - C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 tu ? ? OH Will the first product that forms in this reaction create a new CC bond? Yes No Will the first product that forms in this reaction create a new CC bond? Yes No C $ ©arrow_forwardAs the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C-C bond as its major product: 1. MgCl ? 2. H₂O* If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. This reaction will not make a product with a new CC bond. G marrow_forwardIncluding activity coefficients, find [Hg22+] in saturated Hg2Br2 in 0.00100 M NH4 Ksp Hg2Br2 = 5.6×10-23.arrow_forward
- give example for the following(by equation) a. Converting a water insoluble compound to a soluble one. b. Diazotization reaction form diazonium salt c. coupling reaction of a diazonium salt d. indacator properties of MO e. Diazotization ( diazonium salt of bromobenzene)arrow_forward2-Propanone and ethyllithium are mixed and subsequently acid hydrolyzed. Draw and name the structures of the products.arrow_forward(Methanesulfinyl)methane is reacted with NaH, and then with acetophenone. Draw and name the structures of the products.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
