1. Aldehyde is more reactive towards Nucleophile than ketone.
2. Hydrolysis of acetal gives carbonyl compounds and alcohol.
3. Example of aromatic Nucleophilie substitution by eelimination-addition.
CICI CH3CH2OH 25 °C MT2 Mastery 1 Predict the Product HCI (catalytic) om ". i THF/H20...
please provide mechanism, specifically the first intermediate portion KNH2 NO2 NH3 (liquid) -38 °C MT2 Mastery 6 Provide the structure of first intermediate of the mechanism that leads to this products?
provide the structure of the first intermediate of the mechanism that leads to the product above X 0 Spectroscopy Unknown Pre-tect x G 1-hydroxybutan-2-one Google + C o app.tophat.com/e/170799/assigned reanic Chemistoclecture with MMD (SD201 MT2 Mastery 4 - Image HCI (catalytic) CH3CH2OH mol. sieves 78 °C MT2 Mastery 4 Provide the structure of first intermediate of the mechanism that leads to this products? Type here to search
Please help me with the product LOH HCI (catalytic) THF 65 °C mol. sieves MT2 Master 1 0 Type here to search
show the mechanism + H20 HCI (catalytic) THF mol. sieves 25 °C
predict the products help! t CICI CH3CH2OH 25 °C -SNa (2 equiv.) MeOH 60 °C NO2 НО НСІ (са (catalytic) CH2CH2OH mol. sieves 78 °C
H20 (1 equiv.) HCI (catalytic) ОН THF 65 °C