2. Predict the product for the following transformations (show proper stereochemistry). Pd/C, H2 Me Me Pd/C,...
Predict the (major) product(s), clearly indicating stereochemistry mCPBA Me Me Xs H2, Pd/C CH3 H3C H2, Pd/C Me Draw the lowest energy chair conformer
1. Predict the major product of the reaction. Clearly indicate stereochemistry, if necessary (3 pts) Ph H2 Lindlar cat. hexanes Me 2. Provide reagents to achieve the shown multi-step transformations. (6 pts) Br CH 3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) OME B OMe Me Me NaOH H2O2 Me Me H
predict the product(s) for the following reactions.
Indicate proper stereochemistry when needed. if more than one
stereoisomer forms, draw each one separately.
H2 Pd-C m-CPBA CH2CI NaBH4 CH3OH 1) NaH 2) CH3Br 3) H2 / Lindlar catalyst
PLEASE HELP FAST!!!
1. Predict the major product of the reaction. Clearly indicate stereochemistry, if necessary (3 pts) H 1.9-BBN-H THE Me Me 2. NaOH H202 2. Provide reagents to achieve the shown multi-step transformations. (6 pts) H Me Me Br Br Me Br Br 3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) Ph Li(0) Ph Ph Ph NH30)
predict the products and indicate the relative stereochemistry
for the following transformations. When necessary indicate the
major product.
Me 1. light 2. xylenes, heat Et (d) (4 points) CN xylenes, heat Me 2. H30+, heat 3. Me OH Me Me cat p-TsOH, PhH reflux (d) (4 points) Meo OMe 1. AczO, pyridine Meo 2. HO HO OH
Me 1. light 2. xylenes, heat Et (d) (4 points) CN xylenes, heat Me 2. H30+, heat 3. Me OH Me Me cat...
Hydrogenation of a di-substituted chalcone. Chem 2311.
The catalyst used is excess H2 in 10% Pd/C, and methanol. This
produces 7 different possible products.
Mechanism: a) Propose two advantages of having the palladium metal delivered as a support on carbon instead of using elemental palladium metal? (see p. 148 of the manual for ideas) b) Whether hydrogen is prepared in situ, as in this experiment from ammonium formate, or delivered froma hydrogen gas cylinder, the mechanism of the catalytic reduction...
1) Predict the major product in each of the following
transformations. Show the mechanism.
2) Show how you could synthesize the products below using a
Grignard reagent and appropriate electrophile by drawing the
overall balanced equation. Include the mechanism.
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,сн,МgBr (еxcess) 2. HС{aq) 1. PhMgBr (1 equiv.) 2. HCI(aq) ОН HO 1. CH2MgBr (2 equiv.) 2. HCl(aq) Н Show how...
1) Predict the Products: Using line drawings with proper use of
dashed wedge and solid wedge notation where necessary, draw the
major organic products of the following reactions in the boxes
provided. If no reaction occurs write “no reaction” or “N.R.” in
the box. Include stereochemistry in your answers where appropriate.
If a product is racemic draw both enantiomers or write “racemic”
next to the structure. Assume all reagents written above and below
the arrows are present in excess unless...
Please show mechanisms, thank you.
(Review Topics Draw the product(s) of the following reactions H2 Pd/C CH,CH2-CEC-CH . Consider EZ stereochemistry of alkenes. . If no reaction occurs, draw the organic starting material . Draw one structure per sketcher. Add additional sketchers using the drop-do Separate multiple products using the+sign from the drop-down menu. ChemDoodle
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...