Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s).
Option D, pyrrolidine ,pyridine and workup.
It is an example for Nucleophilic acyl substitution.
Select all the possible reaction conditions that would enable the transformation of the starting material(s) into...
Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s). Question 2 2 pts Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s) ? OCH3 OH a) H2SO4(cat), CH3OH b) work-up a) PBr3, solvent b)work-up a) NaOH, H2O b) work-up a) H2SO 4(cat), H20 b) work-up a) SOCI2, CH30H b) work-up Question 2 2 pts Select all the possible reaction conditions that would...
Question 3 2 pts Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s) CI CI a) NaOCH(CH3)2, solvent b) work-up a) Ethanol, pyridine b)work-up a) NaOH, Methanol b) work-up a) H2SO4(cat), Ethanol b) work-up a) Isopropanol, pyridine b) work-up
Analyze the reaction provided then select all organic molecules that could serve as the starting materials. 0/2 pts Incorrect Question 2 Analyze the reaction provided, then select all the organic molecule(s) that could serve as the starting material(s) of the reaction. a) H2SO4 (cat.), H2o ? b) work-up OH OH OH HO OH OH C A OH OH D C B E A 0/2 pts Incorrect Question 2 Analyze the reaction provided, then select all the organic molecule(s) that could...
Which starting material would best accomplish this transformation? 1. SOCI2 2. CH3NH2 3. LiAlH4 4. H30* Н OH Br Which is the best starting material for the following reaction? CH3CH2NH2 ? pyridine HN o о NH2 С- CI OH Which are the best reagents for the following transformation? OCH3 core O 1. (CH3)2CHMgBr 2. H30+ 1. NaOH, heat 2. (CH3)2CHCH=PPh3 O 1. LiAlH4 2. TosCl, pyridine 3. (CH3)2CHCH Br O 1. DIBAL 2. (CH3)2CHCH=PPh3 What is the major product in...
4. Reaction Fill-ins! Predict the product(s) OR starting material of the following reactions. Remember Hydride shifts are possible if when a more stable carbocation can exist (depending on reaction mechanism)! Put your answers in the indicated boxes. H2SO4 (cat.), H20 а. 1.4-product 1.2-product Br Br HBr b. Br Major product Minor produt Minor product HCI C. 1,2-product 1,4-product HI он MAJOR prod Minor prod. e. Draw the FULL electron-pushing mechanism for the reaction in part a above, INCLUDING ALL resonance...
Establish what is the starting material(s) for the reaction and draw a full mechanism for the following reactions: Establish what is(are) the starting material (s) for the reactions, and draw a full mechanism for the ing reaction. a) NaOH, H2O, HEAT b) work-up Draw a mechanism that explains the formation of the product under the given reaction conditions a) NaOH, H2O b) work-up OH Establish what is(are) the starting material (s) for the reactions, and draw a full mechanism for...
Fill the table with the products of the reaction of the substrated under each set of conditions. Assume a work-up at the end for each reaction. Draw an X through the square of reactions that would not proceed under the given conditions. (Py = pyridine, Ac = acetyl) Assume a work-up at the end for each reaction. Draw an X through the square of reactions that would not proceed under the given conditions. (Py pyridine, Ac acetyl) H2SO4(cat) H20 SOCI2,...
complete the reactions bu adding the starting material, reaction conditions, or all possible products Ph H +Br H- CH3 NaOCH3 DMF Ph Br SK DMF (only product)
Predict the major product(s) , starting material(s) or suggest reagents to carry out the formations depicted below. 11. (30 pts, 3 pts each) Predict the major product(s), starting material(s) or suggest reagents to carry out the transformations depicted below. Your best 10 will count. cat. H2SO4 i. Mg, Eto i. LAH, Eto ii. CO2 iii. H3O+ Bnohd, cat. H2SO4
4. Reaction Fill-ins! Prediet the product(s) OR starting material of the following reactions. Remember, Hydride shifts are possible ifwhen a more stable carbocation can exist (depending on reaction mechanism)! Put your answers in the indicated boxes H,SO, (cat), H,о а. 1,2-product 1,4-product Br Br HBr b. Br Minor produt Major product Minor product HCI C. 1,2-product 14-product HI Он MAJOR prod. Minor prod e. Draw the FULL electron-pushing mechanism for the reaction in part a above. INCLUDING ALL resonance contributors....