
Concept explainers
(a)
Interpretation:
If the given compound must be synthesized using compounds with six or fewer carbons, it is to be determined which carbon–carbon bond-forming reaction from Table 19-1 should be incorporated in the synthesis.
Concept introduction:
The carbon–carbon bond-forming reaction results in heteroatoms having a specific relative positioning along the carbon backbone. If the heteroatoms in a target have 1, 2-, 1, 3-, 1, 4-, or 1, 5- relative positioning and the synthesis calls for a carbon–carbon bond-forming reaction, then consider using a corresponding reaction from Table 19-1. In a retrosynthetic analysis, therefore, apply a transform that takes our target molecule back to reactants. Disconnect the appropriate C-C bond to take back to reactants.
(b)
Interpretation:
If the given compound must be synthesized using compounds with six or fewer carbons, it is to be determined which carbon–carbon bond-forming reaction from Table 19-1 should be incorporated in the synthesis.
Concept introduction:
The carbon–carbon bond-forming reaction results in heteroatoms having a specific relative positioning along the carbon backbone. If the heteroatoms in a target have 1, 2-, 1, 3-, 1, 4-, or 1, 5- relative positioning and the synthesis calls for a carbon–carbon bond-forming reaction, then consider using a corresponding reaction from Table 19-1. In a retrosynthetic analysis, therefore, apply a transform that takes our target molecule back to reactants. Disconnect the appropriate C-C bond to take back to reactants.
(c)
Interpretation:
If the given compound must be synthesized using compounds with six or fewer carbons, it is to be determined which carbon–carbon bond-forming reaction from Table 19-1 should be incorporated in the synthesis.
Concept introduction:
The carbon–carbon bond-forming reaction results in heteroatoms having a specific relative positioning along the carbon backbone. If the heteroatoms in a target have 1, 2-, 1, 3-, 1, 4-, or 1, 5- relative positioning and the synthesis calls for a carbon–carbon bond-forming reaction, then consider using a corresponding reaction from Table 19-1. In a retrosynthetic analysis, therefore, apply a transform that takes our target molecule back to reactants. Disconnect the appropriate C-C bond to take back to reactants.
(d)
Interpretation:
If the given compound must be synthesized using compounds with six or fewer carbons, it is to be determined which carbon–carbon bond-forming reaction from Table 19-1 should be incorporated in the synthesis.
Concept introduction:
The carbon–carbon bond-forming reaction results in heteroatoms having a specific relative positioning along the carbon backbone. If the heteroatoms in a target have 1, 2-, 1, 3-, 1, 4-, or 1, 5- relative positioning and the synthesis calls for a carbon–carbon bond-forming reaction, then consider using a corresponding reaction from Table 19-1. In a retrosynthetic analysis, therefore, apply a transform that takes our target molecule back to reactants. Disconnect the appropriate C-C bond to take back to reactants.

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Chapter 19 Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
- Provide the drawing of the unknown structure that corresponds with this data.arrow_forward20.44 The Diels-Alder reaction is not limited to making six-membered rings with only car- bon atoms. Predict the products of the following reactions that produce rings with atoms other than carbon in them. OCCH OCCH H (b) CH C(CH₂)s COOCH མ་ནས་བ (c) N=C H -0.X- (e) H C=N COOCHS + CH2=CHCH₂ →→arrow_forwardGiven the attached data, provide the drawing for the corresponding structure.arrow_forward
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