intermediate B is less stable than intermediate A because the negative charge is closer to methyl group and methyl group are electron donating group so it increases the electron density at the ortho position to it and account for less stability
Explain the following observations in a concise manner. Use equations, man diagrams and/or resonance structures to...
Explain the following observations in a concise manner. Use equations, mechanisms, diagrams and/or resonance structures to illustrate your answer. i. The following anion (II) spontaneously rearranges to a monocyclic anion with unusual stability. Make sure to include the structure of the rearranged product in your answer. I1 [4 marks The following molecule (II) undergoes umusually facile rotation about the central double bond, whereas "normal" double bonds will not rotate in such a manner. ii. Hас Нс CH3 CHS 14 marks...
Explain the following observations in a concise manner. Use equations, mechanisms, diagrams and/or resonance structures to illustrate your answer. i. The unusual molecule 1,6-methano[10]annulene ( ) exhibits two sets of signals in the 'H-NMR spectrum at 8 = 7.10 (8H) and -0.50 (2H). (4 marks] Compound C is more acidic that compound D. с base [4 marks) Propose a reasonable mechanism for the following reaction of benzene with 1,5-dibromopentane in the presence of a Lewis acid catalyst.
Explain the following observation in a concise manner. Use equations, mechanisms, diagrams and/or resonance structures to illustrate your answer. In a mixture containing the molecules A and B, the labelled methyl groups appear at 8 1.5 and 8-4.2 ppm. Indicate which molecule gives rise to the upfield methyl shift and which molecule gives the more downfield signal Justify your prediction 16 marks Each of the following syntheses will not produce the desired product. In each case, identify the flaw in...