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- Draw the product formed from the ring-closing metathesis of each compound. Then, devise a synthesis of each metathesis starting material using any of the following compounds: CH2(CO2Et)2, alcohols with four or fewer carbons, and any needed organic or inorganic reagents.Fill in the missing reagents a-e in the following scheme:Fill in the missing reagents a-h in the following scheme:
- A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.Draw the product formed from the ring-closing metathesis of each compound. Then, devise a synthesis of each metathesis starting material using any of the following compounds: CH2(CO2Et)2, alcohols with less than five carbons, and any needed organic and inorganic reagents.Draw the product formed from the ring-closing metathesis of each compound. Then, devise a synthesis of each metathesis starting material using any of the following compounds: CH2(CO2Et)2, alcohols with less than ve carbons, and any needed organic and inorganic reagents.
- fill in the missing starting molecule, reagents nessesary or the final major product (s). be sure to include proper sterochemistryDraw the products formed after Steps [1] and [2] in the attached threestepsequence. Then draw stepwise mechanisms for each step.What starting material is needed to synthesize each compound by a ring-closing metathesis reaction?