The most stable carbocation from the following four A -D carbocations is CH3 C A The alcohol that cannot be converted into a carboxylic acid by oxidation or HO OH он A. B C D.

Consider the following dehydration reaction: OH Part: 0 / 2 Part 1 of 2 TSOH How many different structural isomeric products are possible in the given dehydration reaction (assume no rearrangements)? X 5

S14

Draw a structural formula for a hydrocarbon with the given molecular formula that undergoes hydroboration-oxidation to give the indicated product.

Payal

Draw a structural formula for the product of each alkene hydration reaction

6. What is the major organic product obtained from the following reaction? 1. KCN 2. H30*

Alcohols and ethers are more reactive to substitution and elimination reactions under acidic conditions (compared to basic or neutral conditions). Draw the product of the reaction of the molecule shown with a strong acid. O ² ⒸO +1 Which structure from Part 1 would have a better leaving group: the reactant or the product? Choose one: O A. The product would have a better leaving group. OB. The reactant would have a better leaving group. C. Neither structure would have a good leaving group. O D. Both structures have equally good leaving groups. Draw the expected product when the protonated alcohol (the product) from part one reacts with iodide ion. DOC 20+1 H CI Br H C F P Cl Br I

Consider the given alkyl halide with the chemical name, 2-Methyl-2-chlorobutane. What is the major product of the reaction if this alkyl halide was reacted with Ethanol (CH3CH2OH)? Alkyl halide: CH3 H3C ČH3

taken in order to gor the product Please explain the mechanisms/steps