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Chapter 10: Q50 E. (page 308)

Predict the product and provide the entire catalytic cycle for theSuzuki–Miyaura reactions below.

Short Answer

Expert verified

(a)

(b)

Step by step solution

01

Suzuki–Miyaura reaction

Suzuki-Miyaura reaction is an organic reaction, classified as a cross coupling reaction, where the coupling partners are boronic acid and an organohalide, and the catalyst is a palladium complex.

02

Determine Product of the reaction by catalytical mechanism of Suzuki-Mayaura reaction

(a)

Product determination

(b)

Product determination

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Most popular questions from this chapter

Draw structures corresponding to the following IUPAC names: (d) 1,1-Dibromo-4-isopropylcyclohexane.

Tell whether each of the following reactions is an oxidation, a reduction, or neither:

How would you carry out the following syntheses?

How would you prepare the following alkyl halides from the corresponding alcohols?

Alkyl halides can be reduced to alkanes by a radical reaction with tributyltinhydride, (C4H9)3SnH in the presence of light (hv). Propose aradical chain mechanism by which the reaction might occur. The initiationstep is the light-induced homolytic cleavage of the Sn-H bondto yield a tributyltin radical.

R-X+(C4H9)3SnH→hvR-H+(C4H9)3SnX
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