will the Aldol product of this procedure be beta-hydroxyketone or alpha, beta-unsaturated ketone?
We have to make our own procedure so this is all the info I can provide.
Introduction one of the central themes of s In contrasake any synthesis more "green" are a welcome and developing trem Aldol condensation represents a powerful general method for the construction of anic chemistry. In this experiment we will be performi n of 3,4-dimethoxybenzaldehyde and 1-indanone performing a mixed res, this reaction is carried out without solvent. Efforts to reduce to typical ex velopin g trend in modern chemistry. he reaction Experimental-T n: 3,4-dimethoxybenzaldehyde (0.25 g8), 3M HCI (2 mL), sti Partì¤ Given: stirring rod, 1-indanone, NaOH. A lab with glass resent the written group plan to your instructor that outlines how the Aldol reaction objective: 24-dimethoxybenzaldehyde and 1-indanone is to be carried out. Your plan must be approved before proceeding Mix equimolar amounts of with optimal surface area. Be gentle with your stirring. But not too gent Seeing a brown oil is a good thing before the next step. 3,4-dimethoxybenzaldehyde and 1-indanone in a cylindrical vessel Hints: le Add freshly ground NaOH (0.8 molar ratio with the aldehyde) and continue stirig Seeing the mixture turn solid is a good thing. Wait 15 minutes and isolate the crystals using the aqueous 3M HCI (the overall solution must be acidic). How do you check for this? Isolate the crude crystals and dry them in an efficient way (no oven). Record the crude yield before you forget it.