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Draw both combinations of alkoxide and alkyl iodide that are commonly used to try and form the product shown. Circle the pair of reactants that will give the best yield of the products and explain why the other pairs has impaired or no formation of the intended product.

Draw the missing starting material. Reagent 1 is benzene and AlCl3. Reagent B is Zn(Hg) and HCl. Th structure is not isobutyraldehyde

What reagents would I use to produce 1-phenylethanol from 2-phenylethanol?

complete the following synthesis produces using a proper reagent and products

Draw the structures of a Grignard reagent and the corresponding carbonyl compound that could be used to prepare the secondary alcohol shown, using a Grignard reaction approach.

Which of these statements is correct? A) SN1 reactions but not Sy2 reactions create and break a bond to carbon B) Sy2 and E2 reactions create a carbon-carbon double bond C) E1 and E2 reactions must have a Lewis base D) The alkene in electrophilic additions of alkenes is the electrophile E) None of the above statements is correct

From benzaldehyde, compunds of 2 carbons or less, and any inorganic reagent you want synthesize the following compound.

Draw the structure of the major organic product for the following reaction. Cl + NaOCH3

Draw the major organic product for the reaction shown. N. H. HCI, cat.