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

Mechanism: A reaction mechanism for the following reaction is shown below. H+ CEN CEN: N-H || -C-OH H₂O, H* Step 1 wand woled mot ozsm E Step 3 N-H C-OH C=N-H Step2 C=N-H H-O-H H₂O motno vgiene fesrigid onlt to smotnos -C=N-H a) The overall reaction is an example of b) Step 1 is c) Step 3 is d) Draw in the curved arrows for each step. e) Identify the nucleophiles and electrophiles where appropriate. f) Fill in the reaction energy diagram. H₂O: rate determining step to noipojovo hamwell sit 5(emise erit voittons 10) vanas mi sdgin al rainW di of E^ reaction progress →

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 HO

please provide product, mechanism and name of reaction

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Please show the mechanism and product for this reaction

3. 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?

please show the mechanism

Consider 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!!!

Which of the following would be the major product of this reaction? Br t ㅅ H 1 OIV O ||| O II Hint Save for Later Kot-Bu II ||| t IV