Concept explainers
Interpretation:
How to carry out the given synthesis using any reagents necessary, paying attention to the stereochemistry in the target to determine the required stereochemistry of the starting material, is to be proposed.
Concept introduction:
Synthesis may be designed by thinking in the reverse direction, from the product to the starting compound in a method called retrosynthesis. Retrosynthesis involves starting with the product and determining a suitable precursor from which it can be synthesized, without considering specific reactions. The precursor must be a simpler molecule, which may or may not have a close structural relation to the target molecule. This process is repeated until an easily available (or easily prepared) precursor is reached. Each of these steps are called a transform. A synthesis is a specific sequence of
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 (
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Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
- Perform the following synthesis.arrow_forwardSelect one activator & ortho para director to be on a benzene ring to start. You will then add a bromine to this group showing the COMPLETE mechanism, including all resonance structures. Put a box around the stabilizing resonance structure and explain why it is stabilizing.arrow_forwardDraw a mechanism to account for the formation of the NaOH product in the reaction shown here. Hint: Under these A conditions, deprotonation of a propargylic (C=C-CH) carbon is reversible.arrow_forward
- Match each reaction sequence to a product below. Assume any necessary workup. Answers may be repeated.arrow_forwardProvide a multi-step synthesis of the target structure on the right from the starting structure on the left. Indicate the reagents/conditions and the major organic products at each step, do not show any curved-arrow pushing mechanisms. Reactant Problem viewing the image, Click Here Product OHarrow_forwardTBDMS. (SYN) Show how you would carry out this synthesis. Hint: What rearrangement occurs when an enol is formed? ОН ?arrow_forward
- Draw 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_forwardGiven the general reaction coordinate diagram for an El reaction, what does the 1st transition state refer to? TS E TS, SM Reaction Coordinate An activated complex between the leaving group and carbocationic species. An activated complex between the nucleophile and carbocationic species. None of these O An activated complex between the base and carbocationic species.arrow_forwardDraw the detailed mechanism and the product for the following reaction. Be sure to include stereochemistry, if applicable. Brarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning