Part A CH, NaOCH one product HC H Draw the molecule on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars.
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Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.
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- For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOCH3 in CH3OHThe hydrobrominationof 2-methyl-1-butene could theoretically lead to 2 different alkyl bromides; in practice only one product is formed. Draw the structure of both theoretical products, circle the one that is actually produced, and briefly explain whyonly one product forms.(b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants, the transition state, andthe products. Note that the initial product is the salt of an amine (RNH3+ Br - ), which is deprotonated by the excess ammonia to give the amine.
- Explainwhythefollowingdeuterated1-bromo-2-methylcyclohexaneundergoes dehydrohalogenation by the E2 mechanism, to give only the indicated product. Two other alkenes are not observed.Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .the reactions should be all covered in organic chemistry loudon 6 th edition , for exmaple, clemensen/wolf -kishner
- b) Show the mechanism for the radical chlorination of neopentane. Illustrate homolytic bondcleavage and bond formation.What carbon radical is formed by homolysis of the C–Hb bond inpropylbenzene? Draw all reasonable resonance structures for thisradical.Which of A to F would be the major product of the hydroboration/oxidation of the cyclic alkene? can you type instead of handwriting btw or clean handwriting plz
- Provide the E2 mechanism for β-elimination reactionemploying 2-chloro-2-methylbutane to prepare 2-methyl-2-butene and 2-methyl-1-butene reaction. Use the actual structures of thereactants and products. Explain which of the alkenes is the major product ofthis reaction ?Please identify priorities of functional groups and name following molecules based on thier stereochemistry as R or SWhich of the following statement/s is/are false about the reaction of 3-methylhex-3-ene with H3O+?