5,5-dimethylhept-3-ene was reacted with HBr. Provide the reaction mechanism of this reaction.

What is/are the product(s) of the reaction of 2-bromopropane with NaOCOCH3? Draw the mechanism & identify it as Sn1, Sn2, E1, or E2. Please explain your reasoning.

I'm stuck on this one

Predict the product for the reaction between m-ethylbenzoyl chloride (see Problem 20.35) and each of the following. Draw the complete, detailed mechanism for each reaction. If no reaction is expected to occur, write “no reaction." (a) (CH3CH2)2CuLi; (b) LİAIH(O-t-Bu)3, – 78 °C; (c) NaBH4, EtOH; (d) C6H5MgBr (excess), then H*

Please Answer in 30 minutes with handwritten explanation and mechanism !!

The tert-butyl bromide reacts with water with THF as the solvent, as shown in the following scheme: a) Indicate the type of mechanism of this reaction. b) Will the polarity of the solvent affect the reaction rate? c) The solvent that provides the highest speed isTo choose... d) In the case of using water in ethanol, in addition to tert-butanol, a second product. The letter of the product that is formed is: d) If the reaction is done with NaOH solution instead of water and with heating, tert-butanol becomes a minor product. The letter of the majority product of that reaction is:

Clearly label the energy diagram below when answering each part. If there is more than one specific type of label, give an appropriate number afterwards (i.e. Int. 1, Int. 2, etc). State how many step(s) are in the overall reaction, if more than one, clearly label where they start and end Identify the rate determining step (rds) Label all transition state(s) (TS) Label all intermediate(s) (Int.) Label all activation energy(ies) (Ea) Label the heat of the reaction (ΔH) State whether the overall reaction is endothermic or exothermic. please explaing each step. Thank you.