(a)
Interpretation:
The type of acid derivative present, the compound which results from complete hydrolysis and if the given ring aromatic or not is to be explained.
Concept introduction:
Hydrolysis is defined as the phenomenon in which the chemical breakdown of compound is done due to the reaction with water. The aromaticity of the compound is decides on the basis of
(b)
Interpretation:
The type of acid derivative present, the compound which results from complete hydrolysis and if the given ring aromatic or not is to be explained.
Concept introduction:
Hydrolysis is defined as the phenomenon in which the chemical breakdown of compound is done due to the reaction with water. The aromaticity of the compound is decides on the basis of huckel rule. It states that “if a cyclic, planar molecule has
(c)
Interpretation:
The type of acid derivative present, the compound which results from complete hydrolysis and if the given ring aromatic or not is to be explained.
Concept introduction:
Hydrolysis is defined as the phenomenon in which the chemical breakdown of compound is done due to the reaction with water. The aromaticity of the compound is decides on the basis of huckel rule. It states that “if a cyclic, planar molecule has
(d)
Interpretation:
The type of acid derivative present, the compound which results from complete hydrolysis and if the given ring aromatic or not is to be explained.
Concept introduction:
Hydrolysis is defined as the phenomenon in which the chemical breakdown of compound is done due to the reaction with water. The aromaticity of the compound is decides on the basis of huckel rule. It states that “if a cyclic , planar molecule has
(e)
Interpretation:
The type of acid derivative present, the compound which results from complete hydrolysis and if the given ring aromatic or not is to be explained.
Concept introduction:
Hydrolysis is defined as the phenomenon in which the chemical breakdown of compound is done due to the reaction with water. The aromaticity of the compound is decides on the basis of huckel rule. It states that “if a cyclic, planar molecule has
(f)
Interpretation:
The type of acid derivative present, the compound which results from complete hydrolysis and if the given ring aromatic or not is to be explained.
Concept introduction:
Hydrolysis is defined as the phenomenon in which the chemical breakdown of compound is done due to the reaction with water. The aromaticity of the compound is decides on the basis of huckel rule. It states that “if a cyclic , planar molecule has
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Organic Chemistry (9th Edition)
- Write out the expected splitting pattern for hydrogens Ha, Hp and Hc 3Jab = 10 Hz На Hb 3Jpc = 7 Hz CI Hc Hc Ha:Hb:Hc: doublet, quartet, doublet Ha:Hb:Hc: quartet, quartet, triplet Ha:Hb:Hc: doublet, doublet of triplets, doublet Ha:Hb:Hc: doublet, triplet of doublets, doubletarrow_forwardPlease help answer the attached question...thank you!arrow_forward6. Give two reasons why heterocycles undergo electrophilic aromatic substitution reactions faster than benzene even under similar conditions.arrow_forward
- Give detailed Solution with explanation neededarrow_forwardWhich of the following compounds has an activating group? A. Bromobenzene B. Benzoic acid OC. None in the answer OD. Diphenylamine ESTION 2 Which of the following compounds has a deactivating group attached to the benzene ring? OA. Phenol OB. Acetanilide OC. Salicyclic Acid OD. Toluenearrow_forwardIs the product of this reaction more or less soluble than the initial molecule? Why? 1. RCO;H 2. H*, H,O Less water-soluble More water-soluble Water-solubility improved due to a negative charge on the product. Water-solubility improved due to a positive charge on the product. The product now has sufficient H-bonding functional groups to support water-solubility. An acetal has been formed which would decrease the water-solubility Another reasonarrow_forward
- Which of the following is a limitation of the Friedel-Crafts reaction? Select one: O A. The carbocation electrophile can potentially undergo an unwanted rearrangement prior to its bonding to the aromatic ring. OB. Poly-alkylation products form when aromatic reactant and alkylating agent are mixed together in comparable amounts. OC. A Friedel-Crafts reaction fails when the aromatic starting compound contains a moderately or strongly deactivating group. OD. All of the above choices are limitations of the Friedel-Crafts reaction.arrow_forward2. Complete the following electrophilic aromatic substitution reactions for the monosubstituted benzenes, Providing major product(s) only. (Hint: start with identifying the effect of substituent, then figuring out the structure of product) b. C. d. 1. 9₁ ,NO Br CO₂H B1₂ FoBra SO, H₂SO4 EICI AICI Cl₂ FeCl HNO3 H₂SO4 CI Br₂ CH₂COOH 1. SnCl, HyO* 2. H₂O AICI3arrow_forwardWhich of the statements below is true regarding the reactivity of benzene? Select one: a. Being rich in electron, benzene acts as an electrophile in a substitution reaction. Ob. Because of loosely held n electrons, benzene is less reactive than alkene. O . Substitution is preferred over elimination reaction to maintain benzene's aromaticity. O d. The presence of an acid catalyst is added in order to enhance benzene's electrophilicity.arrow_forward
- Arrange the following structures based on increasing reactivity to electrophilic aromatic substitution. CAR OCH₂CH₂CH₂ TAR choose your answer... BAR INCREASING REACTIVITY: choose your answer... COOH JAR choose your answer... V K choose your answer.... Varrow_forward4. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds and any inorganic compounds or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. b. C. CH3 Ph steps Ph CI steps ACHO -CH3 CN steps Ph Ph -OH (racemic)arrow_forwardPlease explain each question.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning