1) Draw 2 different structures that contain carbocations that would undergo a methyl shift a ring expansion Use arrows to show how this would occur
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Q: 1,2 addition of Br2 to an alkene results in a _______________. A. alcohol B. vicinyl dihalide C.…
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Q: Draw the two resonance structures of the carbocation intermediate formed in this reaction. Do not…
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Q: Encircle the most stable alkene. CH3 CH3 CH3 a) CH3 CH2CH3 b)
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Q: Trensproduc is formed 5. Draw the structures of A and B, and use the curved arrow formalism to show…
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Q: 4. Circle any hemiacetal carbons in this molecule. но OH OH
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Q: + 1. Draw line structures of all of the C3H17* carbocations that have the carbon skeleton shown…
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Q: The major product of this reaction exists as two stereoisomers. Draw both isomers. Show all hydrogen…
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Q: in not more than 3 stences, explain why terminal alkynes are acidic do not copy from google i will…
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Q: Draw 2 different structures that contain carbocations that would undergo a methyl shift a ring…
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Q: Draw all resonance structures that result from electrophilic attack at the ortho, meta, and para…
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- Draw a mechanism for the reaction of the ketone with hydronium ion. In the first box, draw any necessary curved arrows. Show the products of the reaction in the second box. Include any nonzero formal charges and all lone pairs of electrons.Draw mechanism for the reactions below. Make sure to show all "electron-pushing" arrows, cond and lone pairs.Draw 2 different structures that contain carbocations that would undergo a methyl shift a ring expansion Use arrows to show how this would occur
- please do only the highlighted qouestionDraw a mechanism for the reaction of methylamine with formic acid. In the box to the left, draw any necessary curved arrows. Show the products of the reaction in the box to the right. Include any nonzero formal charges and all lone pairs of electrons. Finally, check the box to indicate which side of the reaction is favored at equilibrium.So, if I were to have a similar question on an exam, and if it's multiple choice but I'm stuck - I should look for the maximum number of alpha Hs and whichever one is on a tertiary carbocation, correct?
- For the reaction given below, draw a mechanism (curved arrows) and then predict which side of the reaction is favoured under equilibrium conditions.Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all electrons that are necessary to the mechanism and all nonzero formal charges. I did the first step but I'm not sure if it's correct. Don't know what the other steps, if there are, would look like.Can you pleaase answer this?
- Answer the following quesitonDraw the mechanism for the prbolem below! Make sure to include formsl charge, intermediates, and mechanismProvide a complete curved arrow mechanism that accounts for the transformation below. Be sure to show all arrows, reation intermediates, lone pairs, and formal charges