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4 Show how you would accomplish the following synthetic transformations. Show all intermediates.
) cyclodecyne ¡ trans@cyclodecene
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- 1) Make sure to show all intermediates and reagents for the transformation shown below. OH5) What series of synthetic steps could be used to carry out the transformation shown below? Draw intermediate structures and list reagents above/below arrows. a) HO H HConsider the following reaction scheme (note that the reagent shown above the arrow is DBN"). Draw in the expected major product AND indicate what mechanism the reaction will follow. Product: Mechanism:
- Complete the following reactions by providing the missing product(s). Determine what mechanism operates in each case (SN1, Sn2, E1, or E2), Show the stereochemistry of the product(s) where appropriate. If more than one product us formed circle the major one. Br H,O Br NaOCH;CH;Identity reagents that can be used to accomplish each of the transformations show belowDraw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HO
- Show the complete conversion for the two reactions below. If more than one step is required, show the major product for each reaction used. For instance, after each reactant you must show the resulting structure. No need to show the mechanism.Complete the following reactions by providing the missing product(s). Determine what mechanism operates in each case (SN1, SN2, E1, or E2). Show the stereochemistry of the product(s) where appropriate. If more than one product is formed circle the major one.Draw the major product of the following sequence of reactions. If the reaction is likely to give you a mixture of ortho and para disubstituted compounds you should assume that they can be separated; continue the synthesis with either one. If so, draw the intermediates as well. CH3 K₂Cr₂07 Cl₂, AlCl3 H2SO4
- Synthesis: Synthesize the following compounds using the starting material shown a reagents you may need. Show the product after each step. You do not need to shc and I will assume standard work up unless you indicate otherwise. HO, ÕHList all alkene products for each reaction. Write a mechanism for the formation of each product following E1 or E2 mechanisms as appropriate. Be sure to draw arrows for the mechanism.Using curved-arrow notation, drew out the mechanism for the following reaction. Be sure to include stereochemistry and show ail intermediates as well as the final product and include all lone pair electrons. Br₂, H₂O Br Ko OH