For the following dehydrohalogenation (E2) reaction, draw the major organic product. (Cн сок 3 (сн), сон Br Br heat

Draw 2 elimination products

How could you change the reaction conditions given to most strongly favor an E2 mechanism? Br H₂O Use a higher concentration of water Use a stronger base Add a stronger nucleophile O Use a tertiary alkyl halide O Increase the concentration of the reactant

Which mechanism does the following reaction fall into? CI 1) NaNH2, NH3 (liq) 2) H3O+ SNAr (sometimes called addition-elimination) None of the given options Electrophilic aromatic substitution O Elimination-addition NH₂

Draw the product of the E2 reaction shown below. Ignore any inorganic byproducts.

Will the following bases favor an E1 or E2 mechanism?  H2O, CH3CO2^-, tBuO^-, CH3CH2OH, -NH2, NaH

E1, E2, or none?

Which of the following compounds is least reactive in an SN2 reaction? Br -Br E -Br