Question 6. Draw the mechanism of an electrophilic aromatic substitution between the following compound with Cl2. Includes all steps, including the formation of the electrophilic species if required and justify your answer. (Substitution position) using resonance structures. Br OH مینی
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- Why does Hammett Equation only apply to meta and para substituted rings and not others? ExplainWhich of the dompounds is most basic and why?OChem help with the following reaction schemes (see attached image) Please provide the bond line structures for the products obtained in the following reaction schemes... Notice in question #1 that A, B, and C are actually shown as C, B, and finally A in the actual reaction scheme so C correlates with PCC, and so on Question #2 is in order.
- I was wondering, is my answer false? In the book the double bond is p’aced differently than mine, but are they the same or is mine incorrect? If so, how do I know where to place my bonds. The original question was determine the zaitsev or major product.Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction. Be sure to account for all bond-breaking and bond-making steps.Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows.
- Write any specific net reaction of your choice, which represents some type of reaction mechanism that you understand well. You may choose from: nucleophilic substitution elimination electrophilic addition nucleophilic addition nucleophilic acyl substitution. B.) Label what kind of mechanism the reaction is C.) Draw the full curved-arrow mechanism of the reaction, with all resonance structures and formal charges. SHOW EVERY STEP SEPARATELY. D.) Draw the reaction coordinate diagram for the reaction. In it, label the following: Reactants Products Reactive intermediates Transition states (≠) Axes Activation energy ΔG Rate-limiting step ANSWER ALL PARTSNucleophilic attack may appear to occur in two steps as shown below. The alcohol is the nucleophile in this example. It attacks a carbon with a δ+ charge. The second arrow shows the flow of negative charge. WHY is it necessary? The second arrow could be thought of as a resonance arrow. HOW?Write any specific net reaction of your choice, which represents some type of reaction mechanism that you understand well. You may choose from: nucleophilic substitution elimination electrophilic addition nucleophilic addition nucleophilic acyl substitution. B.) Label what kind of mechanism the reaction is C.) Draw the full curved-arrow mechanism of the reaction, with all resonance structures and formal charges. SHOW EVERY STEP SEPARATELY. D.) Draw the reaction coordinate diagram for the reaction. In it, label the following: Reactants Products Reactive intermediates Transition states (≠) Axes Activation energy ΔG Rate-limiting step
- Identify (label) the electrophile and the nucleophile in the reaction and add curved arrows to the following polar reactions to show the flow of electrons:as a follow-up question can explain this mechanismDraw a curved arrow mechanism for the substitution reaction that will occur with the alkyl halide and nucleophile below, adding steps as necessary. Be sure to include all nonbonding electrons and all nonzero formal charges, and show all species that react or are formed in this reaction.