For the following transformations, please provide detailed conditions to give the designated product in maximum yie...
For the following transformations, please provide detailed conditions to give the designated product in maximum yield with minimum by-products. More than one step may be needed. [8 pts eal a) b) MeO он MeO
2. For the following transformations, please provide detailed conditions to give the designated product in maximum yield with minimum by-products. More than one step may be needed. [8 pts ea] o OMe Phoн OH
2. Provide conditions for the following reactions mations for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and stereochemical details. Additionally, if the product(s) listed would exhibit op circle it/them. (14 pts) at would give you the optimum yield, and be mindful of ally, if the product(s) listed would exhibit optical activity, HO + enantiomer in the bord for the com HO
1. Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. (4 pts each) a. H F b. но OH
Problem 6 Provide a detailed arrow-pushing mechanism for the following transformations. (A) 2 Me O OE NaoEt, EtOH Eto, (B) Hint: The cyclohexadienone depicted in the brackets is an intermediate along the reaction pathway to the phenol. 0 315 MeOMe NaoMe, MeOH | MeO₂C CoMe Co-Me Problem 8 Provide a synthesis for the depicted tropinone derivative from the indicated starting materials and any other reagents needed. The best synthesis will require no more than 3 steps. - NH2 Hoza i...
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+ OH CH,OH NaOH Meo NH2 room temp. HO OH Meo Me ОН Meo 2. Provide appropriate conditions to convert each of the following starting mana hexanoic acid (some transformations may require more than one step): It each of the following starting materials into OH OH ОMe "NH₂
Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of 1. stereochemical details. (4 pts each) a b. но ОН For each reaction below, please draw the starting material or the major (singular) product, including any pertinent stereochemical details. (3 pts each) 2. a. 3. Hg(OAc)2, D20 2. KOt-Bu 1.TsCl Он 4. NaBH t-BuOH EtgN etherol b. 3. СHBES 2. LDA 1. HBr KOt-Bu,...
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit.
2. (4 pts.) Provide a reasonable synthesis for the following transformations. More than one step may be needed. Show all reagents and synthetic intermediates.
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit. 2. For the compound shown in the box to the right, provide an IUPAC compliant name, including all stereochemical details.