Create a synthesis that starts from acetylene, benzene, coz, Na cN, NaN 3, of four or fewer and products. or simple alcohol carbons. Show all mechanisms О 0 Br
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- Oxidation reactions can be used in multistep syntheses to produce new functionalities for use in subsequent reactions. Consider the following multistep reaction when you draw the structures in Parts 1 and 2 below. Please explain mechanism's fore the products I and 2 но PCC 1. NaH > Product l Product 2 Br CH,C!, 2. Step 1 Step 2 HOplease provide product, mechanism and name of reactionthisnis the question andwer this correct lly
- Please show the mechanism and product for this reaction3. Show the mechanism for the acid catalyzed addition of H2O to the following ketone. OH H20 CH3 H* 4. The scheme below shows the reaction of a ketone, 2-propanone with methanol. OH :0 : || CH,-C-CH3 : ОН + H CH, c-CH3 CH;-C-CH3 N step 1 step 2 step 3 P CH,OH CH3 CH,OH step 4 + H OCH3 CH,-C-CH3 H - H,0 C-CH3 ÓCH, S CH; step 7 step 6 step 5 OCH3 i) Write the missing structures (N, O, Q and R) in the above reaction scheme. ii) Name the class of compounds P and S belong to? iii) This is an acid catalyzed reaction. What does this statement mean? iv) Draw the arrow diagram in step 6 to show how intermediate R is formed? Write the equation for this step ONLY. v) Steps 3 and 7 involve loss of a proton from the intermediate ions. Why is this step necessary?Predict the products for the following reactions by showing complete reaction mechanisms. Also, identify the nucleophilic attack, loss of leaving group, proton transfer, rearrangement in the mechanism steps. Show curved arrows in the reaction mechanisms.
- please show the mechanismConsider the following reaction: AIC Toluene MECOCI Me- COME TICI How are these products being formed? Show all appropriate steps (mechanism) in this reaction. Show all appropriate arrows!!!State the mechanism of the following reactions (NOTE: draw theproper settings where applicable)
