6. What would happen to the rate of the reaction below under the following conditions? (Use textbook for assistance. Circle the correct answer.) H₂O Хон a) Increasing the concentration of water? b) Decreasing the concentration of the halide? c) Changing the leaving group to bromine? d) Starting with 2-iodopropane? INCREASE SAME DECREASE INCREASE SAME DECREASE INCREASE SAME DECREASE INCREASE SAME DECREASE
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- Arrange the given alcohols in order of reactivity in an acid catalyzed dehydration reaction. O Hold and drag to reorder Fastest = 1. Second fastest = 3. Slowest = 2. OH OH HO 1) 2) 3)Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is that they tend to be contact explosives What quailities make alkyl diazonium salts such excellent leaving groups?Draw the reaction mechanism for the reaction between an aldehyde and water under acidic conditions. (H') H,0
- How to complete these reactions...I need help very confusedQuestion 8 Identify the sequence of curved arTOWs (electron movement) in the steps of the following reaction. H. :Br: (A) proton transfer, nucleophilic attack (B) loss of leaving group, proton transfer C) loss of leaving group, rearrangement (D loss of leaving group, nucleophilic attackComplete the following stepwise reaction mechanism problems based on the reaction conditions given: Draw the stepwise mechanism.
- 6). What do you think would be the better nucleophile? Cu Organocopper reagent Cu Organocuprate reagentHow is the rate of the reaction affected when concentrations of both nucleophile and alkyl halide are doubled for SN' reaction? (A) rate is doubled B) rate remains the same c) rate is tripled D rate is quadrupled(4 times)Use the appropriate reagent used in the reaction. (d),(e) please!!
- Consider the SN2 reaction of butyl bromide with OH- ion. CH3CH2CH2CH2B + OH- → CH3CH2CH2CH2OH + Br Assuming no other changes, what effect on the rate would result from simultaneously doubling the concentrations of both butyl bromide and the OH- ion? Draw the curved arrow mechanism for the SN1 reaction of methanol with tert-butyl iodide. Next, draw an Energy vs. Reaction Coordinate diagram for this reaction, labeling all transition states as "TS" and intermediates as appropriate for those drawn in the mechanism above, showing the relative energies on the diagram.Draw the organic product of the nucleophilic substitution reaction. Include all hydrogens atoms. CH³CH₂I + CH³CH₂O¯ Select Draw с Rings O H I More + Erase DOutline syntheses. Beginning with the starting materials indicated, OUTLINE a reaction efficiently makes the product named. Use any other materials you need. Outline: reactants, reagents, conditions, sequence that products (major, minor); NO MECHANISTIC DETAIL.