
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Draw the structure of each of the organic precursors in the following two-step synthesis.

Transcribed Image Text:Br2
NaNH2
Draw the precursor to the final alkyne product. Assume excess NaNH2 followed by an acid workup.
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- Provide a multi-step synthesis of the "Final Product" from the given "Reactant" by completing the synthesis scheme below. Draw the entire synthesis scheme & complete the synthesis scheme and box your answers as shown below. Indicate the set of reagents/conditions #1, #2, and Draw the chemical structure of major organic product at each step i.e. Compounds A, B, and C. Each set of reagents/conditions may contain more than one reagent. Use the notation 1., 2., etc., to show the steps in each set of reagents/conditions as appropriate. Do not show any curved-arrow pushing mechanisms. (Reactant) Final Product TSOH HO OH Compound A Reagents/Condition(s) #1 Compound B MOTHE Reagent(s)/Condition(s) #2 Compound Carrow_forwardIdentify an alkyne precursor for each of these molecules, along with the reagent(s) needed to convert the alkyne precursor to the target. Draw the precursor molecule write the reagents over the arrow.arrow_forwardDraw the content of the final reaction mixture. Explain your reasoning.arrow_forward
- Draw the mechanism of how you can make cyclohexyl ethanoate from ethanearrow_forward8) Consider the below desired transformation. Develop a retrosynthesis and forward synthesis that would successfully accomplish it. شدم مشهدarrow_forwardComplete synthesis, include reagents and intermediate compounds. If functional group needs to be protected, show.arrow_forward
- 8) Consider the below desired transformation. Develop a retrosynthesis and forward synthesis that would successfully accomplish it. doarrow_forwardSynthesise the target molecules drawn below using precursor chemicals within the following limitations: 1) ALL intermediates and reagents must be shown.2) Each molecule requires multiple step synthesis.3) You must also synthesize any organometallic reagents or ligands that you wish to use. a) Aspirin is a common pain killer that was developed by Bayer.arrow_forwardDraw a mechanism for the following reaction (see image).arrow_forward
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