12. For the following reaction, predict the product (s). Include appropriate stereochemistry No mechanism necessary. (8...
5. Draw an arrow-pushing mechanism for the following reaction, and predict the stereochemistry of the product(s). If more than one stereoisomer is formed, state which stereoisomers will be formed in equal quantities and which will be formed in unequal quantities. cat. H2SO4 HO Draw an arrow-pushing mechanism for the following reaction, and predict the stereochemistry of the product(s). If more than one stereoisomer is formed, state which stereoisomers will be formed in equal quantities and which will be formed in...
Predict major product Predict the product(s) of the following Diels-Alder reaction. Include stereochemistry if appropriate OCH CHO
2. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (primary, secondary, or tertiary alkyl halide), nucleophile (strong or poor), and the solvent type (protic or aptrotic). Specify the type of reaction mechanism (SN1 or SN2), show the curved arrow mechanism and draw the products as 3D structures to illustrate stereochemistry. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (1º, 2º, or 3 alkyl halide). mucleophile (strong or poor),...
1. Predict the major substitution product(s) for the following reactions. Include stereochemistry if appropriate. You may assume an aqueous workup is performed after each reaction. 1. Nah, DMF ТОН 2. Mel BrMg-Ph KCN 16 { ad ton ot MeOH HD Na Br Me DMSO EtOH Br ~ Br DMSO * Me OH LNH2 M HO Me-S (1 equiv) Me DMF
In each reaction Predict the major organic product(s). Where necessary show appropriate stereochemistry and regiochemistry. DO NOT DRAW THE MECHANISM! 1) Br/FeBr 2) Separate p-isomer 3) CH3CH2B(OR)2/PdL2/NaOH 4) KMnO4/NaOH/A 5) H 0 1) Br2/FeBr3 2) Separate p-isomer 5) H30 3) CH3CH2B(OR)2 4) KMnO4/NaOH/A PdL2/NaOH C. C.
1. Predict the product(s) of the following SN2 reactions and include stereochemistry where necessary. Br КОН NaOCH DMSO
Q: For a-f, predict the product. Write out the reaction and include stereochemistry, when needed. a. Alcohol and NaH and subsequent reaction with an alkyl halide b. Alkyne and NaNH2 and subsequent reaction with an alkyl halide c. Reaction of alcohol and a sulfonyl chloride (to make a sulfonate ester), and a subsequent reaction d. of the product with another reagent e. Reaction of alcohol and thionyl chloride a subsequent reaction of the product with another reagent) f. Reaction of...
2. Predict the products for the following reaction. Show stereoisomers formed and me mechanism of the reaction. 3. Predict the major product for each of the following reactions. Show the mechanis indicate stereochemistry where appropriate. BR be H.0 Tommi OH 11)
8) Predict the product(s) of the following E2 reaction. Be sure to include solid wedges and dashed es on your product(s). Use conformational structures (the templates below) to show the mechanism and explain your reasoning Br CHCH ONa CH CH2OH, 70 °C Explanation(s): 9) Consider the E1 reaction of (3S)-3-bromo-2,3-dimethylpentane to form alkenes a) Draw the structure of the haloalkane (be sure to include stereochemistry). Clearly label any chiral carbon atoms with an asterisk ). b) Draw the structures of...
Q: For a-f, predict the product. Write out the reaction and include stereochemistry, when needed. a. Alcohol and NaH and subsequent reaction with an alkyl halide b. Alkyne and NaNH2 and subsequent reaction with an alkyl halide c. Reaction of alcohol and a sulfonyl chloride (to make a sulfonate ester), and a subsequent reaction d. of the product with another reagent e. Reaction of alcohol and thionyl chloride a subsequent reaction of the product with another reagent) f. Reaction of...