(a)
Interpretation:
From the given compounds, the compound with high regioselective ability towards addition of
Concept introduction:
Addition Reaction: It is defined as
The product of electrophilic addition reaction obtained by addition of electrophile to
Electrophile: Electrophiles are electron deficient compounds which accepts electrons from nucleophiles that results in bond formation.
Leaving group: it is a fragment that leaves substrate with a pair of electrons via heterolytic bond cleavage.
Chemical reaction involves bond making and breaking of two or more reactants in order to attain products from the reactants.
Cation: The positively charged chemical species is referred as cation.
Regioselective reaction: They are reactions which contain more than one product which are actually molecules with same molecular formula but different in the way they are connected and among those products only one product is major.
(b)
Interpretation:
From the given compounds, the compound with high regioselective ability towards addition of
Concept introduction:
Addition Reaction: It is defined as chemical reaction in which two given molecules combines and forms product. The types of addition reactions are electrophilic addition, nucleophilic addition, free radical additions and cycloadditions. Generally, compounds with carbon-hetero atom bonds favors addition reaction.
The product of electrophilic addition reaction obtained by addition of electrophile to
Electrophile: Electrophiles are electron deficient compounds which accepts electrons from nucleophiles that results in bond formation.
Leaving group: it is a fragment that leaves substrate with a pair of electrons via heterolytic bond cleavage.
Chemical reaction involves bond making and breaking of two or more reactants in order to attain products from the reactants.
Cation: The positively charged chemical species is referred as cation.
Regioselective reaction: They are reactions which contain more than one product which are actually molecules with same molecular formula but different in the way they are connected and among those products only one product is major.
Want to see the full answer?
Check out a sample textbook solutionChapter 6 Solutions
EBK ORGANIC CHEMISTRY
- Which of the following does not undergo conjugate addition with butanamine? a. Propenal b. But-2-enal c. But-3-enal d. Butenonearrow_forwardWhat is the answer for a,c,d,e,g and h?arrow_forwardWhat contributes to the deactivating nature of halides inelectrophilic aromatic substitution? a. inductive effect b. octet rule c. delocalization of electron pairarrow_forward
- 4, 11:59 PM Which option is the major product expected for the reaction below? a. b. C. 00 d. N 1) KCN 2) HCI (slow addition) " Narrow_forward2. For each pair of the following compounds, identify which compound and conditions would react more rapidly in SN2 reaction? Briefly explain the deciding factor. A. B. C. F Loti L Br OTf KOH methanol CI KOH acetonearrow_forwardPurine is a heterocyclic compound with four nitrogen atoms. a. Which nitrogen is most apt to be protonated? b. Which nitrogen is least apt to be protonated?arrow_forward
- Do dicarbonyls or ketones react faster? Explain whyarrow_forwardA mixture contains equal amounts of compounds A–D. a.Which compounds alone are optically active? b. If the mixture was subjected to fractional distillation, how many fractions would be obtained? c.How many of these fractions would be optically active?arrow_forwardGive the IUPAC or common name for each compound. (A - E)arrow_forward
- Using the resonance theory which carbocations is more stable ? And why ?arrow_forward1. a. 4-methoxybenzoic acid is less or more polar than 4-methoxyacetophenone? explain why (WITHOUT DRAWINGS) b. 3′-chloro-4′-methoxyacetophenone is less or more polar than 4-methoxyacetophenone? explain why (WITHOUT DRAWINGS) 2. a. 4-methoxybenzoic acid has a higher melting point than 4-methoxyacetophenone. explain why? (WITHOUT DRAWINGS) b. 3′-chloro-4′-methoxyacetophenone has a higher melting point than 4-methoxyacetophenone. explain why? (WITHOUT DRAWINGS)arrow_forwardHow could 1H NMR spectroscopy be used to distinguish between each pair of compounds?arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY