write full mechanism a. CH3OH + H+ + CH3OH2+ H НО- носин сне + CI- b....
Are these conformational isomers?
OH CI H. CH3 НО, CH3 CI CH3 H2C H CI CI
Draw a reasonable mechanism for this reaction: H-CI NH HO H-: но NH3
5. Circle the better a) acid CH3OH CHiNH or b) nucleophile in protic solvent CI or c) base CH3S CH3O or 6. Write out the mechanism for the following elimination reaction. Show all steps am arrows, Be sure to show all organic products, indicating which is major/minor. Br H2O+ 7. Write out the mechanism for the following reaction. Show all steps and use cur НО +Br2
What will be the product of this reaction? CI H2O CI acetone 요 ОН ОН НО НО. А B о ОА ов ос о There will be no reaction Which of these is the correct mechanism for the substitution of tert-butyl chloride? H Hot Hot H ta - Hot - Но c) toinen Hot Hot OA ос
3 of 15 A reaction proceeds by the following mechanism: 1. CH4+Cl2-CH3+HCI+CI 2. CH3+Cl2-CH3CI+CI What is the overall reaction? CH4+2Cl2-CH2CI+HCl+2C1- CH4+HCI-CH3CI+H2 OCH4+2Cl2-CH2Cl2+2HCI CH3+C1--CH3C1 4 of 15 Which reaction mechanism is consistent with the overall reaction, 2NO2+F22NO2F? O 1. NO2+F2-NO2F+F 2. NO2+FNO2F O 1. 2NO2-N204 2. N204+F2-NO2F+NO2+F O 1. NO2+F2-NOF+O+F 2. NO2+F=NOF O 1. NO2+F2-NO2F2 2. 2NO2F2-2NO2F+F2
how many transition / intermediate states?
# CH, CH3 НО * / -OH + H-CI step 1 step 2 step 3
give the FULL detailed mechanism for each reaction
Etz & CH3OH b) TsOH + H20 gulo CALOR NpSOHO PhH 64%
draw the major product
14. HNO, CHO Но+н H-HOH H-HOH HO+H CH2OH 15. oo HNcO; 1) (CH3),COCOCOC(CH3) 3 o N:C:NH/ Ph сно HOTH PHNHNH2 16. HOH (3 equiv.) H +OH HO+H CH2OH
Draw the mechanism for the following reaction
НО НО ОН НО ОН НО. Н. [H+] EAS [н'] EAS
3. Provide a full arrow-pushing mechanism for each of the following reactions. Но, он НО Но он і - H- 0ң но он Насо, осна Нt H2O 4. A researcher wants to run the following sequence of reactions. However, they know starting Grignard reagent cannot exist due to the presence of its reactive carbonyl group. MgBr H.H cannot exist! An acetal group can be used to protect" a carbonyl from attack, allowing it to survive otherwise incompatible reaction conditions. Provide...