Concept explainers
Interpretation:
The synthesis of the target molecule from the given starting material is to be determined.
Concept introduction:
Retrosynthetic analysis involves considering the reaction sequence in reverse. The analysis starts with the product determining the precursor that can produce it when the reaction is carried out in the forward direction. The retrosynthesis step, called a transform, does not consider a specific reaction or reaction conditions for the reaction in the forward direction. The transform is represented by an open arrow (
The synthesis in the forward direction is then determined on the basis of the structural differences and the
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Organic Chemistry: Principles And Mechanisms
- Draw the complete, detailed mechanism for the following reaction, and predict the major product. NaCI MeOHarrow_forwardDraw the complete, detailed mechanism for the reaction shown here and give the major product. CH3I (excess) ? NH2arrow_forward(SYN) Show how you would carry out the following synthesis using any reagents necessary. Hint: The synthesis may require more than one synthetic step.arrow_forward
- (SYN) Show how to carry out each of the following syntheses, using any reagents necessary. Hint: In each case, the carbonyl group of a ketone or aldehyde is entirely removed. (a) (b) ? OCH3 OCH3 OCH3 OCH3 (c) (d) ? ? OH Pharrow_forward(SYN) Show how to carry out each of the following transformations. (a) (b) ? ? OH CIarrow_forwardCN (SYN) Propose how to carry out the synthesis shown here using any reagents necessary. ? CNarrow_forward
- (SYN) Suggest how you would carry out the synthesisshown here using any reagents necessary. Hint: Thesynthesis may require more than one synthetic step.arrow_forwardProvide a complete, detailed mechanism for the reaction CH;CH,OH shown here.arrow_forwardDraw a complete, detailed mechanism for the reaction shown here.arrow_forward
- (SYN) Show how to carry out the transformation at the right, and draw the complete, detailed mechanism for НО that reaction. НО Но OH ОНarrow_forwardDraw the complete, detailed mechanism for the reaction shown here, and explain why nucleophilic attack takes place predominantly at the epoxide carbon that is attached to the vinyl group. HCI H,0 ОН 63%arrow_forward(SYN) Show how to make each compound from an alkene. (a) (b) OH HOarrow_forward
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