Draw the major product of the given alcohol dehydration in the presence of H, SO. Use the Zaitsev rule (no rearrangements) to predict the major product when necessary. Include all hydrogen atoms.
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- Draw the major organic product formed in the following reaction.Consider the reaction of an alkyl bromide with water. Draw the neutral organic products.Draw the major product of the given alcohol dehydration in the presence of H, SO,. Use the Zaitsev rule (no rearrangements) to predict the major product when necessary. Include all hydrogen atoms. Select Draw Rings More Erase CH3 H2SO4 H H3C-CH2-ć-C-C-CCH3 + H,0 ČH3 ÓH
- How many unique ether products will be formed when the following reaction is performed? Draw the product of the above reaction that has six carbon atoms and an ether functional group. Be sure to include all lone pairs of electrons.Draw the starting reactant that would produce this alcohol when treated with this reagent. Ignore inorganic byproducts.Draw the major organic product formed in the reaction.
- Draw out a complete arrow-pushing mechanism for the following reaction. This reaction is explicitly done with heat. O NaOH, H₂O heatAcetal product formation requires an acid catalyst in the second step, but NOT in the first step. True or False?Why is it not advisable to use aqueous hydrochloric acid in a Grignard reaction of a ketone? A) The Grignard reagent will react with the acid and cannot react with the ketone. B) The ketone will be protonated and will become unreactive. C) The ketone will form an unreactive enol. D) The Grignard reagent won't dissolve in aqueous solutions
- Draw the structure(s) for the major final product(s) formed in the following reaction sequence. CN ༼་་ SO 503 H₂SO4 Cl FeCl3 Click and drag to start drawing a structure.Give the IUPAC name (including any E,Z designation) for each unsaturated aldehyde.Draw the products of homolysis or heterolysis of each attached indicated bond. Use electronegativity differences to decide on the location of charges in the heterolysis reaction. Classify each carbon reactive intermediate as aradical, carbocation, or carbanion.