Concept explainers
(a)
Interpretation: The products formed by the reaction of
Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.
Answer to Problem 23.47P
The product formed by the reaction of
Explanation of Solution
The given compound is,
Figure 1
The nucleophile
Figure 2
On the further treatment of
Figure 3
Hence, the product formed by the reaction of
The product formed by the reaction of
(b)
Interpretation: The products formed by the reaction of
Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.
Answer to Problem 23.47P
The product formed by the reaction of
Explanation of Solution
The given compound is,
Figure 4
The nucleophile
Figure 5
On the further treatment of
Figure 6
Hence, the product formed by the reaction of
The product formed by the reaction of
(c)
Interpretation: The products formed by the reaction of
Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.
Answer to Problem 23.47P
The product formed by the reaction of
Explanation of Solution
The given compound is,
Figure 7
The nucleophile
Figure 8
On the further treatment of
Figure 9
Hence, the product formed by the reaction of
The product formed by the reaction of
(d)
Interpretation: The product formed by the reaction of
Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.
Answer to Problem 23.47P
The products formed by the reaction of
Explanation of Solution
The given compound is,
Figure 10
The nucleophile
Figure 11
On the further treatment of
Figure 12
Hence, the products formed by the reaction of
The products formed by the reaction of
Want to see more full solutions like this?
Chapter 23 Solutions
ORGANIC CHEMISTRY
- Draw the products formed when each compound is treated with HNO3 and H2SO4.State whether the reaction occurs faster or slower than a similar reaction with benzene.arrow_forwardProvide all possible products formed in the given reaction Draw the products formed when each ether is treated with two equivalents of HBr.arrow_forwardSynthesize the following compounds starting with benzene and any other inorganic reagents. 4 a. H2N Br b. O2N с.arrow_forward
- Enols are quite reactive toward electrophiles than alkenes because: а. The OH group has a powerful electron-donating O resonance effect b. A resonance structure can be drawn that places a negative charge on one of the carbon atoms, making this carbon electrophilic С. The enol can react with nucleophilic carbon to form a new bond to carbon d. None of the options are correctarrow_forwardDraw the product formed when each starting material is treated with LDA in THF solution at −78 °C.arrow_forwardHow can the following compounds be prepared using ethyne as the starting material?arrow_forward
- The reaction of a nitrile with an alcohol in the presence of a strong acid forms an N-substituted amide. This reaction, known as the Ritter reaction, doesnot work with primary alcohols. a. Why does the Ritter reaction not work with primary alcohols? b. Provide an explanation for why an amide is less susceptible to nucleophilic attack than its corresponding ester.arrow_forwardShow how each of the following compounds can be prepared from methyl phenyl ketonearrow_forwardproduct formed by treating butanal with 1. AgNO3 in HH3 2. Acidified K2CrO4 3. LiAlH4arrow_forward
- What Wittig reagent and carbonyl compound are needed to prepare each alkene? When two routes are possible, indicate which route, if any, is preferred.arrow_forwardCompound that is most easily hydrolyzed by acid in water `NH A. В. F C. D.arrow_forwardDraw the organic product(s) formed when CH3CH₂CH₂OH is treated with each reagent. a. H₂SO4 d. HBr g. TsCl, pyridine b. NaH h. [1] NaH; [2] CH₂CH₂Br e. SOCI₂, pyridine f. PBr3 c. HCI + ZnCl₂ Hint: NaH deprotonates the alcohol forming an alkoxidearrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning