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- 4. Synthesize the following compound. You may use benzene, acetylene, ethanol and any inorganic reagents. O₂NFrom benzene, organic compounds with 6 carbons of less and any other inorganic compund you want. Synthesize the following naphthalene derivative.Propose a synthesis of the following molecule starting with benzene. Be sure to show all reagents and products formed along the way. You do NOT need mechanisms here.
- 4) We discussed in class how acetals are formed from a ketone and two equivalents of an alcohol, using an acid catalyst. Alternatively, would a strong base also catalyze (i.e. accelerate) the formation of an acetal? Explain why or why not, in the context of the reaction mechanism and potential intermediates. Naome, MeoH าาาา ← meo ome + HzoAldehydes and ketones react with thiols to yield thioacetals just as they react with alcohols to yield acetals. Predict the product of the following reaction, and propose a mechanism:Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.
- How would you synthesize 3-hexyne using ethane as your only carbon source? You may use any reagents.propose a synthesis for the following molecule starting from benzene. There is no need to show the mechanism, just show all reagents and conditions that need to be used on each stepA Q2 Provide products. Br₂ AgNO3 H₂0
- Answer the question in full details and complete paragraphs, using lots of information about the topic and your own knowledge, do not plagiarize!Hiii!! Can somebody here help me with what my tutor made me? I can't really understand it completely. Thank you!Suggest a step by step mechanism for this reaction.