Interpretation:
Whether each step in the given mechanism is reasonable or not is to be determined. An explanation is to be given for any steps that are not reasonable.
Concept introduction:
Reasonableness of a multistep mechanism and the individual steps in it are evaluated on the basis of a few rules. Proton transfer reactions must be compatible with the reaction conditions. Strong acids cannot exist under basic conditions and strong bases cannot exist under acidic conditions. Proton transfer reactions are very fast compared to other reactions, so they can be added at any stage as long as they are compatible with the conditions. An intramolecular proton transfer is generally not reasonable, particularly if the solvent is acidic or basic. In this case, a solvent mediated proton transfer is more likely. Another important rule is related to the number of species that participate in an elementary step. Typically only one or two species react in a given step. Steps containing three or more molecules/ions are extremely rare, and therefore unreasonable. In an

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Chapter 8 Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
- Would the following organic synthesis occur in one step? Add any missing products, required catalysts, inorganic reagents, and other important conditions. Please include a detailed explanation and drawings showing how the reaction may occur in one step.arrow_forward(a) Sketch the 'H NMR of the following chemical including the approximate chemical shifts, the multiplicity (splitting) of all signals and the integration (b) How many signals would you expect in the 13C NMR? CH3arrow_forwardDraw the Show the major and minor product(s) for the following reaction mechanisms for both reactions and show all resonance structures for any Explain why the major product is favoured? intermediates H-Brarrow_forward
- 3. Draw ALL THE POSSBILE PRODUCTS AND THE MECHANISMS WITH ALL RESONANCE STRUCTURES. Explain using the resonance structures why the major product(s) are formed over the minor product(s). H₂SO4, HONO CHarrow_forward7. Provide the product(s), starting material(s) and/or condition(s) required for the No mechanisms required. below reaction HO + H-I CI FO Br2, FeBr3 O I-Oarrow_forward6. Design the most efficient synthesis of the following product starting from phenot Provide the reaction conditions for each step (more than one step is required) and explain the selectivity of each reaction. NO MECHANISMS ARE REQUIRED. OH step(s) CIarrow_forward
- What is the skeletal structure of the product of the following organic reaction?arrow_forwardIf a reaction occurs, what would be the major products? Please include a detailed explanation as well as a drawing showing how the reaction occurs and what the final product is.arrow_forwardWhat is the major organic product of the following nucleophilic acyl substitution reaction of an acid chloride below?arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning

