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Answer for the number 8 question, Thank you. No need for long explanation.
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- 1 example for organic rearrangement reaction show: a. the overall reaction (reactants --> products) b. the reaction mechanism (indicate intermediate product) c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?) d. overall description of the reaction eg., radical substitution or SR1 example for organic elimination reaction show: a. the overall reaction (reactants --> products) b. the reaction mechanism (indicate intermediate product) c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?) d. overall description of the reaction eg., radical substitution or SR1 example for organic substitution reaction show: a. the overall reaction (reactants --> products) b. the reaction mechanism (indicate intermediate product) c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?) d. overall description of the reaction eg., radical substitution or SR
- Do problem 31, any other problem on the worksheet or 341 example of reaction for each of the types of organic reactions: substitution, elimination, addition, and rearrangement. Show:a. the overall reaction (reactants --> products)b. the reaction mechanism (indicate intermediate product)c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?)d. overall description of the reaction eg., radical substitution or SRFor 10.29, the trans product (major product) and the cis product (third product) are displayed as possible E2 products. However, for 10.30, only the trans product (major product) is shown. How come the cis product is not needed?
- 1. Of the two unimolecular reactions shown, decide which you think would be faster, i.e., which would have a higher relative rate constant (krel)? 2. Based on your answer, draw two lines on one reaction coordinate diagram that show the relative progress of each reaction along its path to product indicated? 3. what is Bond dissociation energy of the C-LG bond? 4. what is the Nature of the leaving group (LG)? 5. what is the relative size of activation energy (Ea) for each reaction? 6. what is the Hammond's postulate? 7. what are the Relative thermodynamic stability of the reactive intermediates? 8. what is Influence of the solvent (if given) on the reactions and intermediates?Please help me making a sheet look like the 1st picture for ethane using alkenes, alkenes, alkynes but it should only have the reaction shown in second picture please make it loke a sheet ASAPShow full curly arrow mechanims and please talk about regioselctivity/stereoselctivity. Also, define which one is nucleophile, electrophile, base/acid/reducing agent and reaction name. Please draw a new one. Thank you
- Consider the reaction in the picture. Determine the product/s during: a. Initiation b. Termination c. Propagation1 example for organic addition reaction show: a. the overall reaction (reactants --> products) b. the reaction mechanism (indicate intermediate product) c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?) d. overall description of the reaction eg., radical substitution or SRdo not fully undsertand the slide,need further explanation. what does it means by the additive effect of two group?which two group ??why OH is a more powerful activator than CH3? meta rarely take please because it is too hindered?why too hindered?Too hindered in EAS or which reaction?why??I am confused.