2. Propose an appropriate set of starting material and reagents to synthesize the target molecule below via the Williamson Ether Synthesis. Use numbered steps where appropriate. alcohol ot ок

Please help me with this organic chemistry question.

3. Propose a synthesis for the target molecule from the provided starting material. You may use any additional reagent with four carbons or less as required.

Propose a reasonable stepwise mechanism, using curved arrow notation to show the flow of electrons, for the following reaction. O₂N H KCN EtOH, H₂O O₂N OH NO₂

Show how to  complete the following synthesis.  can use all reagents and as many steps needed

Predict the major product of the given reaction and then draw a reasonable mechanism for the product formation using appropriate curved arrow notation. Part 1: OH H2SO4 (aq) view structure Part 2 out of 4 H,0 H,SO4 HSO, HO finish structure . draw structure . H;O*

. Provide a mechanism for the following reaction. H cat. HO HO H₂O OH O-H T →

Fraw the lower and higher molecular weight

Synthesize the following ether from any two alcohols. YOU MUST SHOW the complete retrosynthetic analysis as well as the reagents you would use in the forward direction.

please,don't provied handwriting solution.