Concept explainers
Interpretation:
A mechanism for the acid catalyzed α-substitution reaction in which
Concept introduction:
In the presence of aqueous acids ketones tautomerize to their enol forms. The nucleophilic displacement of the chloride ion of selenyl chloride by the attack of the double bond of the enol and the subsequent deprotonation yields the product required.
To propose:
A mechanism for the acid catalyzed α-substitution reaction in which ketones react slowly with benzeneselenyl chloride in the presence of HCl to yield α-phenylselenoketones.
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OWLv2 with Student Solutions Manual eBook, 4 terms (24 months) Printed Access Card for McMurry's Organic Chemistry, 9th
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- given cler asnwerarrow_forwardAdd curved arrows to the reactants in this reaction. A double-barbed curved arrow is used to represent the movement of a pair of electrons. Draw curved arrows. : 0: si H : OH :: H―0: Harrow_forwardConsider this step in a radical reaction: Br N O hv What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. O primary Otermination O initialization O electrophilic O none of the above × ☑arrow_forward
- Nonearrow_forwardCan I get a drawing of what is happening with the orbitals (particularly the p orbital) on the O in the OH group? Is the p orbital on the O involved in the ring resonance? Why or why not?arrow_forward1) How many monochlorination products-including stereochemistry- are there for the molecule below:arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning