give the structure of the major alkene formed when N-ethyl-N,N-dimethylbutylammonium hydroxide is heated. If more than one product can be formed, indicate which is the major product and explain why.
give the structure of the major alkene formed when N-ethyl-N,N-dimethylbutylammonium hydroxide is heated. If more than...
Give the products formed in each reaction. If more than once alkene product forms, indicate which once predominates. If stereoisomer products form draw 3D representations. + HD CI 4 : 's O - C 4, C H. y 7 Br 3M. Nt D lig w H , , Br C=H + HO: #*,
why is n- butyl chloride more reactive that ethyl iodide which is more reactive than ethyl bromide?
formulas of all chloro that u when treated with KOH to give the following alkene as the major product. . Do not show stereochemistry in other cases. . Separate structures with + signs from the drop-down menu. ChemDoodle OWLv2 I Onine t are two dias s of 3-b ethoxide in xene as the major diastereomer gives the E alkene, and the other gives the Zalkene. Which diastereomer gives the E alkene? Me Me Me Br Me Et Et Et Following...
Part A Draw the product formed when the structure shown below is heated with ruch NBS is N-bromosuccinimide. Interactive 3D display mode
If more than one is product is formed indicate which is major. Full regio and stereo rules now apply. CH,CH,CH=CH, (ether) HBr XCHI СРВА 1.BH OH CH 2.H,O,.HO 10-4444 - H , CHỊCH, CH, Pd CHH CH.CH
Predict the major organic product for each reaction below. Predict the structure of the alkene you would use to prepare each alkyl halide below (only product The reaction of isobutene with HBr in ether gives one of the two products below as the major product. Answer the following question(s) about this reaction. HBr Br + ether Product A Product B 32. Which product would be the major product? 33. Which product would be formed via a primary carbocation?
Draw the structure of the product formed when the following compound is heated in aqueous base. The formula for the product is C8H12O.
can question 7.58 and 7.69 be answered please 7.6 7.58 When (R)-3-bromo-2,3-dimethylpentane is treated with sodium hydroxide, four different alkenes are formed. Draw all four products and rank them in terms of stability. Which do you expect to be the major product? 7.59 When 3-bromo-2,4-dimethylpentane is treated with sodium hydroxide (NaOH), only one alkene is formed. Draw the product and explain why this reaction has only one regiochemical outcome. educed when each of the
Answer them accordingly thank you! Question 1 a) Give the mechanism for the reaction below: 3-ethyl-3-methyl-1-pentene + HBF3-bromo-3-ethyl-2-methylpentane b) The questions are based on the reaction scheme as shown below: H202 BH3 NaOH, H20 i) Determine the structure of intermediate A and product B. ii) The formation of product B follow one rule in electrophilic addition. What is the name of the rule and explain that rule. i) Give one reagent that can be used to reduce the alkyne above...
Draw the major organic products of the reaction. (Hint: might there be more than one product? Will it be only substitution, only elimination, or some of each?) Indicate the stereochemistry, including H's, at each stereocenter. Omit byproducts such as salts or methanol. If there is more than one alkene that can form, only draw one of them, the one that forms to greater extent. CH3ONa CH3OH 1111