Draw the structures of all the possible products that can be obtained from the dehydration of 2-methylcyclohexanol. Using curved arrows, write a detailed mechanism to show how each product is formed. Indicate which product would be the major one.
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- Acetal derivatives of aldehydes and ketones are prepared by an acid-catalyzed dehydration reaction with alcohols or diols. Using more pictures than words, draw a reaction and a mechanism that shows the formation of acetal.draw a correct mechanism to react with 2-methylocta-4,6-dien-1-amine with the given reagent. Again, disregard any parts of the molecule represented by R-groups and focus on the given portion of the molecule. Be sure the correct mechanism arrives at the correct product of the reaction. The incorrect mechanism may or may not have the correct productDraw the reaction mechanism for the reaction between an aldehyde and water under acidic conditions. (H') H,0
- Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism must account for all the products if more than one product is formed. 4-methycyclohexanol with phosphoric acid H3PO4 to for 1-methycyclohexene, 3- methylcyclohexene and 4-methycyclohexeneAddition of water to an alkyne gives a keto‑enol tautomer product. Draw the ketone that is in equilibrium with the given enol.In a Wittig reaction, a ketone or aldehyde reacts as an electrophile with a nucleophile called a Wittig reagent (or phosphonium ylide) to produce an alkene. The Wittig reagent is commonly synthesized first in a two-step process beginning with an alkyl halide, then reacted with the carbonyl compound. In this problem, you'll explore the mechanism of a multi-step synthesis to make an alkene using the Wittig approach.
- Hydroxylamine, H2NOH, has both an OH functional group and an NH2 functional group, so it can feasibly undergo reaction with a ketone or an aldehyde to produce either an acetal or an imine-like compound called an oxime. (a) Draw each of these mechanisms for the reaction of hydroxylamine with acetone. (b) Which is the major product? Hint: Which step decides the outcome?For the following step in a reaction, use arrows to show how the end product is achieved.-Methylbutanal undergoes an aldol reaction to form 3-hydroxy-2-isopropyl-5-methylhexanal. Additional heating in base will form the aldol dehydration product. 10% NCH 5°C Step 1: add curved arrows. Select Draw Templates Mar |||||||||||| M Complete the mechanism for the dehydration reaction by adding missing honds and curved arrows. Draw the aldol dehydration product in the last step. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the tructure, use the undo button in the lower-left corner of the panel to reset the structure 3 Ć НО Era Q2Q Step 3: complete the structure of the product. Select Draw Templates Mar XTZ ? 10-1 Q2Q Step 2: complete the structure and add curved arrows. Select Draw Templates More ||||||| Era AND heat