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a)
Interpretation:
Whether the electrocyclic reaction shown takes place in conrotatory or disrotatory manner is to be stated. The conditions, thermal or photochemical, under which the reaction can be carried out also is to be stated.
Concept introduction:
In elecrocyclic reactions involving even number of electron pairs, a thermal reaction occurs in conrotatory manner and a photochemical reaction occurs in disrotatory manner.
In elecrocyclic reactions involving odd number of electron pairs, a thermal reaction occurs in disrotatory manner and a photochemical reaction occurs in conrotatory manner.
b)
Interpretation:
Whether the electrocyclic reaction shown takes place in conrotatory or disrotatory manner is to be stated. The conditions, thermal or photochemical, under which the reaction can be carried out also is to be stated.
Concept introduction:
In elecrocyclic reactions involving even number of electron pairs, a thermal reaction occurs in conrotatory manner and a photochemical reaction occurs in disrotatory manner.
In elecrocyclic reactions involving odd number of electron pairs, a thermal reaction occurs in disrotatory manner and a photochemical reaction occurs in conrotatory manner.
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Chapter 30 Solutions
EBK ORGANIC CHEMISTRY
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- man Campus Depa (a) Draw the three products (constitutional isomers) obtained when 2-methyl-3-hexene reacts with water and a trace of H2SO4. Hint: one product forms as the result of a 1,2-hydride shift. (1.5 pts) This is the acid-catalyzed alkene hydration reaction.arrow_forwardNonearrow_forward. • • Use retrosynthesis to design a synthesis Br OHarrow_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
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