Provide detailed (arrow pushing) mechanism for the following reaction. Where appropriate indicate Lewis acid and base for each step, and whether they are also Bronsted acids and bases (LB/BA, LA/BA etc.) Indicate the number of steps in the mechanism and the number of intermediates. HO OH H₂O HCI (cat)
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Provide detailed (arrow pushing) mechanism for the following reaction. Where
appropriate indicate Lewis acid and base for each step, and whether they are also
Bronsted acids and bases (LB/BA, LA/BA etc.) Indicate the number of steps in the
mechanism and the number of intermediates.
Step by step
Solved in 1 steps with 1 images
- Give a clear explanation handwritten answer...complete the following reactionA. For the following reaction, give a full curved-arrow pushing mechanism for formation of BOTH products and indicate the Lewis acid and base at each step ( LA or LB ) and whether they are also Bronsted acids and bases (BA or BB). Include all reasonable resonance contributors for any intermediates AND INDICATE THE MAJOR RESONANCE CONTRIBUTOR IF APPROPRIATE B. Indicate which product, A or B, would be formed under thermodynamically controlled conditions and which would be formed under kinetically controlled conditions and give a BRIEF explanation of the role of temperature in determining kinetic and thermodynamic control C. Draw a reaction energy diagram for both reactions on the same diagram.Which of (a)-(d) shows the increasing order of basicity of compounds 1-4?
- Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Arrange the intermediates below in order of increasing basicity:Electrostatic potential maps of anisole and thioanisole are shown. Which do you think is the stronger acid, p-methoxybenzoic acid or p-(methylthio)benzoic acid? Explain.Hi, My question is " What is the acidity order of this compounds and explain why?"