Propose a reasonable mechanism for the following reactions.
Given Reaction:
Mechanism:
An unshared electron pair of pyran is treated with 2-bromomethyl-5-nitrophenol to form a conjugated acid by SN2 reaction.
The unshared electron pair of hydroxy group is reacted with conjugated acid to form oxonium ion.
The H2O molecule abstracts a proton from the conjugated acid to give a final product.
Propose a reasonable mechanism for the following reactions. Show charges.
1. Provide a reasonable mechanism to account for the following
reaction.
3. Propose a reasonable mechanism for the following
reactions.
7. Propose a mechanism for the formation of the
following products.
NO2 H2SO4 HNO; Br Br AICI: + CI Br FeBrz AICI: -CI
The second one
1. Propose a reasonable mechanism for each of the following reactions: A. AIC1 CI ook Ai
Propose a reasonable arrow-pushing mechanism for the following
transformations. (Organic Chemistry, Synthesis)
4. Propose a reasonable arrow-pushing mechanism for the following transformations. Br Br2 ど。 OH H2SO4 H20 OH
Outline a reasonable mechanism for following reactions:
7. outline a reasonable mechanism for the following reactions: H heat benzene
19. Propose a reasonable mechanism for the reactions below. If resonance stabilized intermediates are generated, draw its contributor(s). a. он он H20 b. он NaOH Br Br
1. Draw the product structure and propose a reasonable mechanism for the following reactions: NBS, H,0 DMSO C,H,OBT 1. BH, THE 2. H2O2, OH
3. Propose a reasonable stepwise mechanism for the following transformation. (10 marks). Cu
3. Propose a reasonable stepwise mechanism for the following transformation. (10 marks). Cu
4. Draw a reasonable mechanism for the following
reactions
4. Draw a reasonable mechanism for the following reactions TOH heat Ho* NaOH (aq) igro montant gro heat
4. Propose a plausible mechanism for each following
reactions:
4. Propose a plausible mechanism for each following reactions: "COOH conc. H2SO4 c. 1. BH3. THE 2. H2O2, NaOH, H2O 3. NaH 4. CH3Br Ph