Aldol reaction product is beta hydroxy carbonyl compound.
Aldol condensation reaction product is alpha-beta unsaturated carbonyl compound.
3. Provide the product for the intramolecular aldol reaction below. (1 point) i NAOH NaOH
3. Provide the product for the intramolecu lar aldol reaction below. (1 point) NaOH 4. Provide the starting reagents for the aldol condensation reaction below. (1 point) NaOH H 5. Provide the product for the reaction below. (1 point) Br NaOH + Br
1. What is the major organic product obtained from the following intramolecular aldol condensation reaction? NaOH, HẠO . 1 b. 2 . 3 d. 4 2. What is the major organic product obtained from the following intramolecular Claisen Condensation (Diepkova ) reaction? مع عمه Baraeenie Product onlained from ( 1. NaOCH2CH3 CH3CH2OH CH3CH30 OCH2CH3 2. H30+ OCH CHE OCH2CH3 مسلسلا سلال OCH2CH3 OCH2CH3
4. Provide the starting reagents for the aldol condensation reaction below. (1 point) NaOH NaOH.
Predict the product of the following intramolecular Aldol reaction. NaOH, HAO Δ H ४१.स
Predict the product of the following intramolecular Aldol reaction NaOH, H & H O O O me
9. Give the major organic product of each intramolecular Aldol reaction. NaOH, H2O heat NaOH, H2O b. H heat NaOH,H,O NaOH, H2O heat 168
please answer all of the 4 questions
What cyclic product is formed in the intramolecular Aldol condensation when the following compound is treated with aqueous NaOH? OT 11 0 0 IV What is the Aldol addition product formed from reaction of the following compound with itself? ++,C#o Cาถวาย 0 0 0 What is the cyclic product formed in the intramolecular Aldol condensation when the following compound is treated with aqueous NaOH? 08 pod od IV OT O II III O...
5. Provide the product for the reaction below. (1 point) Br NaOH
which of the following molecules cannot undergo an
intramolecular aldol condensation when treated with NaOH
Which of the following molecules cannot undergo an intramolecular aldol condensation when treated with NaOH
answer all questions if possible.
VI. Pre-Lab Problems 1. Draw the complete curved-amow mechanism for the base-catalyzed aldol com adol condemnation to form dehydrorheosmin (or dehydrozingerone) from acetone ar (or dehydrozingerone) from acetone and 4-rwydroxybenzaldehyde for varwin) (2 points) HGH HO Ho7 - o nucophilic Atau dehydration 2. Describe at least two different limitations to the aldol reaction. (1 point) 3. Provide the product for the intramolecular aldol reaction below. (1 point) i i NaOH. 4. Provide the starting reagents...