Concept explainers
Interpretation:
The given order of reactivity has to be accounted.
Concept Introduction:
The increasing stability order of carbocation is as follows,
Primary carbocation < secondary carbocation < tertiary carbocation
Nucleophile: Nucleophiles are electron rich compounds which donates electrons to electrophilic compounds which results in bond formation. Nucleophilic nature depends on the negative charge present in the molecule, the solvent in which it present and the electronegativity of the atom.
Leaving group: it is the fragment that leaves the substrate in a
Want to see the full answer?
Check out a sample textbook solutionChapter 21 Solutions
Organic Chemistry
- Establish the reaction and propose a mechanism for the reaction of benzene with bromine catalyzed with ferric bromidearrow_forwardProvide the products of the reaction of 1-propene with HBr in the presence and absence of peroxide. Explain the mechanism of the formation of the products in detailarrow_forwardProvide the necessary sequence of reactions to generate the products below from their respective starting materials.arrow_forward
- Styrene (vinylbenzene) undergoes electrophilic aromatic substitution much faster thanbenzene, and the products are found to be primarily ortho- and para-substituted styrenes.Use resonance forms of the intermediates to explain these results.arrow_forwardAcid-catalyzed hydrolysis of the following epoxide gives a trans diol. Of the two possible trans diols, only one is formed. How do you account for this stereoselectivity?arrow_forwardPropose a pericyclic mechanism to account for the following transformation:arrow_forward
- Enamines normally react with methyl iodide to give two products: one arising from alkylation at nitrogen and the second arising from alkylation at carbon. For example, Heating the mixture of C-alkylation and N-alkylation products gives only the product from C-alkylation. Propose a mechanism for this isomerization.arrow_forwardPropose and illustrate detailed mechanisms to complete the following reactionsarrow_forwardDiphenylacetylene can be synthesized by the double dehydrohalogenation of 1,2-dibromo-1,2-diphenylethene. The sequence starting from (E)-1,2-diphenylethene consists of bromination to give the dibromide, followed by dehydrohalogenation to give a vinylic bromide, then a second dehydrohalogenation to give diphenylacetylene.(a) What is the structure, including stereochemistry, of the vinylic bromide?(b) If the sequence starts with (Z)-1,2-dibromo-1,2-diphenylethene, what is (are) the structure(s) of the intermediate dibromide(s)? What is the structure of the vinylic bromide?arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning