In the first step, alkene gets protonated and forms carbocation. since the carbocation is not stable (Generally oxygen attached carbon will not bear positive charge) it undergoes another resonance contributor where positive charge bearing on the oxygen atom. Then bromine anion was attacked sp2 carbon to give the product.
Draw the structure(s) of the carbocation intermediate, including resonance contributors, to show why this is the case.
2. Using resonance contributors for the intermediate carbocation, explain why a phenyl group is an ortho-para director. FeCl3 + Cl2
Draw the resonance contributors to the carbocation CH3CH(+)CH=CHCH2CH3 Does the ion have a symmetric structure? *the plus sign is on the second carbon
Draw the significant resonance contributors for the cations. Draw the significant resonance contributors for the cations shown below: I H. N
Any help would be appreciated Draw the 3 resonance contributors for the cation intermediate of the reaction below. HNO3/H2SO4 NO2
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.
Draw both resonance structures of the most stable carbocation intermediate in the reactions shown.
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.
Draw all the resonance structures for the stabilized carbocation intermediate formed in the following SN1 reaction. 2. CH3 CH3 OH H+ Nuc Nuc Ph Ph
Draw the best Lewis structure, and resonance contributors of equal energy (if any), for the molecule XeOF4. Answer the following questions based on your Lewis structure(s). 1- draw Lewis structure 2. Select the VSEPR shape that best describes the shape about the central atom Xe in this molecule/ion? Linear Trigonal Planar Tetrahedral Trigonal Bipyramidal Octahedral 3. Select the molecular shape that best describes the shape about the central atom Xe in this molecule/ion. Linear Bent (109.5) Bent (120) Trigonal Planar...