Which compound would not undergo a decarboxylation reaction using H30* and heat? 0 0 elan ollen...
state whether or not these compounds would undergo
decarboxylation.
State whether or not these compounds would undergo decarboxylation reaction when heated, and if they would - draw the product of the decarboxylation reaction.
Question 2 (1 point) Saved Which set of hydrogen atoms will undergo deuterium exchange with MeOD in the presence of MeONa? 1 2 1 and 2 only O2 and 3 only O 2 only O 3 only Which would be a reasonable intermediate for the this reaction? H30* PhoMe Ph-Me Ph Ome PhẩOMe OH PhẩOMe + OH OH + H2 Question 4 (1 point) Which hydrogen is most acidic? ace OD Question 5 (1 point) What is the product of...
Which acid group would most easily undergo decarboxylation? e. HOC d. CO2H HOQC CO2H a. C. CO2H b. a. Ob O c. O d. Oe.
13. Select the key step for the mechanism of decarboxylation: 0 HO OH Оме HO H2SO4 OME Me product O'HO A В. D 14. Which reagent(s) is(are) needed to complete the desired synthesis?: 0 ? A. NaOme MeO H dil. HCI B. NaOH, CHO} heat C, LDA, (MO) CO / MCPBA D. CO, heat
major product of the reaction below would be... OEt 1) NaOEt 2) BrCH2CH2CH3 3) H30, heat Select one: O a. ОН ob. DH OC O= Od
Which compound would undergo the fastest dehydration on treatment with H2SO4?
Predict the product of this reaction: o H30+ OH heat
The compound below can undergo a double dehydration reaction
with potassium bisulfate at high temperatures. Draw the major
product of the first (compound A) and second (compound B)
dehydration steps for this molecule.
он KHSO4 heat НО, А В Х СЕ) СЕ) С6Н120, C6H100 ОН Н,0 Н,0
10. Select the compound that can not be made using the malonic ester synthesis: O O OH MeO Оме OH Ph OH A. B. Ph C. D. 11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A. the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel D....
10. Select the compound that can not be made using the malonic ester synthesis: O o O OH MeO OMe OH Ph ОН A. B. Ph C. D. 11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A. the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel...