Here, in all the reactions, base is given and one carbonyl
compound is also given. So 1st base forms enolate ion by taking
alpha proton of carbonyl. Then this enolate attacks on the another
molecule of same compounds carbonyl grp.. To form bita hydroxy
carbonyl compound.. On condensation H2O removed and enone will be
formed.
QUESTION 5 O OEt OEt I + 2 O OEt Ph ОН Ph Ph Ph OH A B с Et OEt H2O Ph nto Et Ph nto OEt D E F Select the two products that will form in the reaction outlined above. ОА OB OD ОЕ OF
What is the major product of the following reaction? NH2OH EtOH OH OH NHOH ONH2 OEt OH OH
O HO Et OH Ph NMe on Ph Et Ph OH Ph OEt Ph A B с D E OET o O O-Et OH Ph OEt Ph Et Ph NH2 Ph Ph F G H J From the list of structures above, select the product for each reaction and enter the letter in the box. For these reactions, assume excess reagent is available to react with the organic compound. o Ph + ОMe EtMgBr 5 0 Ph CI + EtOH...
Propose a synthesis
5. Propose a synthesis B OH OEt OE K OB
4. Which one of the following compounds is a ketal? OH OEt E C B
O HO Et OH Ph NMez Et Ph ОН Ph OEt Ph A B с D E OEt O 0 Et 0- OH Ph OEt Pn Et Ph NH2 Ph Ph ד G H I From the list of structures above, select the product for each reaction and enter the letter in the box. (Assume aqueous workup when needed.) O + Ph NaBH 1 O + CH,Li Ph Н. 2 Product 1 Product 2
Identify reagents that can be used to accomplish the following
transformations.
OH OEt Etl [H']. EtoH, -H20 H2SO4, H2O 2) EtOH Eti OH H'] EtOH, -H20 H2SO4, H20 2) EtoH 1NaOH 2)Etl OH PCC OH H]. EtOH, -H20 2) EtOH Etl OH Na2Cr20 H2SO, H2O H']. EtOH, -H20 EtOH
Y EtOH 01) OEt 2) OEt Eto > + O 3) OEt Eto o 4) OEt 'OEt
9. Ph CH3 MeOH, H+ 10. -CEN CHO 11. NH2 CEN 12. O OET OH
QUESTION 6 OET -CH3 Et Et + OH OH Et Select the major product (or no reaction) and mechanism for the reaction above. Compound A Compound B Compound Compound D No Reaction S1 E15N2 E2 QUESTION 7 Br Me OCH, Et oh + O MeOH Ph Ph Select the major product (or no reaction) and mechanism for the reaction above. Compound A Compound B Compound C Compound D No Reaction SN 1 SN2 E2