2.41 Draw the products formed from the acid-base reaction of H₂SO, with each compound. a. -OH b. NH₂ OCH3 d. N-CH₂

Complete the reactions given below

Give the IUPAC or common name for each compound.

Identify the major product for each of the following El reactions: ? он ? EIOH Heat Br conc. H,SO, Нeat (b) OH Br conc. H,SO,, 2 Heat ? EIOH Heat (c) (d)

Reaction A. NaOEt EIOH Incorrect Reaction B. (CH3,COK (CH3,COH Incorrect

What steps are needed to convert A to B?

What is the product in the following reaction? Li/Liq.NH3,t-BuOH ? m-CPBA (1eq.) OMe (В) (A) OMe OMe (C) (D) OMe OMe

Provide the required information for the reaction scheme below: OH Compound B Compound C OH Compound A CHO CH2OH CHO CH2OH Compound E Compound D

QUESTION 2 The following is a proposed synthetic strategy that uses one starting alcohol in two separate single-step reactions (I and II) to make a pair of diene and dienophile which together undergo a Diels-Alder reaction to give a Diels-Alder product. The Diels-Alder product is subsequently converted to the final ether in a three-step synthesis (III, IV and V). Identify the reagent(s) from Table I required for each of those three sysnthese and place the number (A1, A2 reagent(s) in the given box right next to the corresponding step numbers (I to V) of the synthesis. DO NOT fill in any box with more than one number. (Note: This question is different from the previous synthesis question which allows two numbers for each box). You will be graded based on the number in each box. Do not fill in any single box with more than one number. Do not leave any box blank. B1, B2..., or C1, C2 ...) that represents the (I) diene OH (III, IV and V) Diesl-Alder product (II) dienophile Table I Number…

Ff.323.