Which of the following is an effective way to complete the synthesis below. NH₂ 1) NaOH 2) CH3NH₂ 1) LDA 2) NaNO3 1) NH3 2) H3O+ 1) HNO3/H2SO4 2) H₂/Pt/Ethanol (can't reduce ring)

draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions.

Which of the following compounds reacts faster in an elimination reaction with KOH? Also provide the major product(s) (if any) for each elimination reaction. Br Br )...

from compound 3 to 4, the nitro group in compound 3 is going through [ hydrolysis / reduction / substitution / oxidation] to afford compound 4

please answer in text form and in proper format answer with must explanation , calculation for each part and steps clearly

Hello, If you could please help me solve this problem. These are the options for each reagent.  1:  HCl/H2OHCl/H2O CH3NH2CH3⁢NH2 NaOH/H2ONaOH/H2O methanol 2:  NaOH/H2O CH3NH2 methanol HCl/H2O 5. NaOH/H2O CH3NH2 methanol HCl/H2O 6 NaOH/H2O CH3NH2 methanol HCl/H2O

Please don't provide handwritten solution

Draw the MAJOR organic product(s) for each of the following reactions/sequence of reactions. OEt ΕΙΟ OEt OH 1) PCl3 / Br₂ NH2 2) / pyridine 1) EtONa / EtOH 2) H3O+ (dilute) 1) EtONa / EtOH 2) Ph 3) NaOH / H₂O Br 4) H2SO4/H₂O/heat OH 1) SOCI₂ 2) HO- / Et₂N NO2 1) MCPBA / CF3SO₂H 2) Ph-NH2/pyridine 1

Provide the major organic product in the reaction below. H OH H POCI3 pyridine

Can you please tell me the reagents/conditions of each step 1, 2, 3 and possible occuring problems (for example: side reaction)? If there's any issues, please explain why the step works well.