Step 1 Step 2 Step 3 Step 4 i Draw H3CH2C¯, and then add the curved arrow notation showing a nucleophilic addition.

Draw the full mechanism for this reaction. Show all proton transfer steps.

Please correct answer and don't use hend raiting

after you write the five reacitons pathways, label the rate-determining step and mechanism please

Show a possible pathway and include all intermediate and reagents.

Show the mechanism for the given reaction conducted at -5 °C in CCI,. cyclohexene + bromine → dibromocyclohexane Draw structures, including charges and electrons, and add curved arrows. Details count. Draw each species (organic and inorganic) resulting from the previous step. Then, add curved arrows for the forward reaction. Include charges and nonbonding electrons. Add curved arrows to the first step. : Br - Br : Draw the major product. Include charges and nonbonding electrons.

Please help with these and include the steps in the reaction so i can better understand how they work! just 1 or two of them is fine

None

Using the curved arrow to guide your reasoning, draw the other product of this dissociation reaction.

The substitution reaction studied here with Chlorobutane and KOH is known to have a second order rate equation meaning the transition state in the slow step involves both nucleophile and electrophile. Knowing that, which of the following statements are true? Select all that apply. A) Adding more Chlorobutane (the electrophile) will not change the rate of the reaction. B Adding more KOH (the nucleophile) will make the reaction go faster. Adding more Chlorobutane (the electrophile) will make the reaction go faster. D) Adding more KOH (the nucleophile) will not change the rate of the reaction. E Adding more KOH (the nucleophile) will make the reaction go slower.