(10) EXTRA: Propose a mechanism to explain the following result. A completely correct answer will account...
1. Provide a reasonable mechanism to account for the following reaction. 3. Propose a reasonable mechanism for the following reactions. 7. Propose a mechanism for the formation of the following products. NO2 H2SO4 HNO; Br Br AICI: + CI Br FeBrz AICI: -CI
Propose a mechanism to account for the observed product VII. (10 pts) For EITHER TWO of the four reactions below, propose a mechanism to account for the observed product. Mechanism means showing every step of the transformation, and showing arrows (movement of electrons). 1) Nah (base) 2) 2-bromopropane DMF HBr
Please explain in full detail. 8. (10 - extra credit) (a) (6) Propose la 2-4 step mechanism to explain this conversion. OH (b) (4) Draw a reasonable reaction coordinate diagram for this process.
PLEASE ANSWER EVERYTHING Using curved arrows, propose a mechanism for the following reaction. In addition, draw in all lone pair of electrons and positive charges that are needed. Finally, label the Lewis acid, Lewis base, nucleophile, and electrophile in each step. acid catalyst Paraldehyde(a sedative and hyptonic agent)
5. Propose a reasonable mechanism to account for the following reaction. (5 pts) H2O/H2SO4
Propose a mechanism to account for the following: Would it be optically active? Page 4 of 16 5) (20) a) Propose a mechanism to account for the formation of the following observed reaction product(s) 1) NaBH4 CH3CH2OH 2) H30* он
6. Propose a mechanism and predict the product for the following reaction. Be sure to include resonance structures. (10 points) OCH AICI, 10 7. Provide the products for the following reactions (12 points) Bra. fuming FeBry H2SO4 AICI
Please Answer Both questions Propose a mechanism for the following reaction under conditions that favor a SN1 reaction. HO -ОН Br For the following reactions provide the mechanism and explain the relative relate of the reactions. KOC(CH3)3 rel rate = 1 Br trans KOC(CH3)3 rel rate > 500 Br cis
4. Propose a synthetic pathway for the following reaction (there may be more than one correct way), then show the mechanism for each step (Hint: To save time make sure your synthesis pathway is absolutely coret before you work on mechanism) но Br
Please answer all two questions and please explain! I'm completely lost at the moment and I'm not sure how to solve it. Please do it step by step if possible. 10. (10 points) Account for the relative product distribution for the radical bromination reaction shown below. (a) Write the hydrogen abstraction step reaction (radical formation), including the transition state, that leads to each product. (b) Match each reaction to the correct reaction coordinate diagram. Draw the reactants on the energy...