raw the major organic product formed when the compound shown below undergoes a reaction with Bra Interactive 3D display mode

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For each reaction in question 20, sketch a reaction coordinate energy diagram indicating the starting materials, transition states and any intermediates, if present, in the reaction. Don't worry about the absolute energy of starting materials and products but you can assume that the product is more stable than the starting materials.

Consider the reaction conditions provided in the question(s) below question. Determine the type of reaction that will occur. Identify the role of potassium tert-butoxide in this reaction. Br KOtBu tBuOH A) strong base B) weak base or nucleophile C) electrophile D) solvent

PLEASE, I DO NOT UNDERSTAND THIS QUESTION. STEPS LEADING TO THE CORRECT ANSWER WOULD BE HELPFUL! BOND LINE DRAWINGS PLEASE.

Predict the products of this organic reaction: CH3 CH₂ || No reaction CH3 | O−CH–CH2–CH3 + KOH A Specifically, in the drawing area below draw the structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. Click anywhere to draw the first atom of your structure. X Ś Ć

6) You have decided to repeat the reaction from Question 5 using a slightly different alkene starting material. You now observe 3 products, and you suspect that your major product (Product A) is the result of a carbocation rearrangement. Draw the mechanism for the formation of Product A and indicate which type of carbocation rearrangement has occurred. H₂O H₂SO4 A OH 67% Major Product B OH 32% Minor Product C 1% OH

Draw the product formed when the compound shown below undergoes a reaction with HCI in H₂O. Interactive 3D display mode H3C CH3

The overall dehydration reaction we are performing (the dehydration of cyclohexanol) is reversible and actually slightly endothermic. How can we shift the equilibrium to the product side, assuming we can not limitlessly increase the temperature?     Increased magnetic stirring     le Chatelier's principle     Increased amount of catalyst     Extended reaction time

Hello, I do not understand these two questions, can I please get help? Bond line drawings would be helpful, please!