Concept explainers
(a)
Interpretation:
With
Concept Introduction:
Suzuki reaction: It involves coupling of an aryl, a benzyl or vinyl halide with organoborane in presence of
Alkyl boranes are generated by hydroboration of
Retro synthesis: It is a technique of planning an
(b)
Interpretation:
With
Concept Introduction:
Suzuki reaction: It involves coupling of an aryl, a benzyl or vinyl halide with organoborane in presence of
Alkyl boranes are generated by hydroboration of alkynes in presence of reagent namely catecholborane.
Retro synthesis: It is a technique of planning an organic synthesis by the reverse approach. In this technique, the starting materials are obtained by cleaving the target molecule into logical synthons. Synthons are precursor fragments of the target compound when it is cleaved. Depending on the stability, the synthons are classified as logical and illogical synthons. Logical synthons are highly stable precursor fragments, and illogical synthons are less stable precursor fragments of the target compound.
(c)
Interpretation:
With
Concept Introduction:
Suzuki reaction: It involves coupling of an aryl, a benzyl or vinyl halide with organoborane in presence of
Alkyl boranes are generated by hydroboration of alkynes in presence of reagent namely catecholborane.
Retro synthesis: It is a technique of planning an organic synthesis by the reverse approach. In this technique, the starting materials are obtained by cleaving the target molecule into logical synthons. Synthons are precursor fragments of the target compound when it is cleaved. Depending on the stability, the synthons are classified as logical and illogical synthons. Logical synthons are highly stable precursor fragments, and illogical synthons are less stable precursor fragments of the target compound.

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Chapter 23 Solutions
Organic Chemistry
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