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What product would you expect if cinnamaldehyde and acetone reacts?
The reaction of cinnamaldehyde and acetone typically results in the formation of 2'-Hydroxychalcone, also known as butein. Butein is a natural chalcone derivative that has been studied for its various biological activities, including antioxidant and anti-inflammatory properties.
What is the mechanism for the aldol condesation reaction of acetone and p-anisaldehyde?
In the aldol condensation between acetone and p-anisaldehyde, the p-anisaldehyde first acts as the electrophile, accepting a proton to form an enolate ion. This enolate ion then attacks the carbonyl carbon of acetone, forming a new carbon-carbon bond. The resulting aldol product undergoes dehydration to form the final α,β-unsaturated ketone.
What type of reaction is acetone reacted with triiodomethane?
An iodoform reaction is the type of reaction when acetone reacts with triiodomethane.
What is the solvents used to dissolve cinnamaldehyde?
Common solvents used to dissolve cinnamaldehyde include ethanol, acetone, and ethyl acetate. These solvents are effective in dissolving cinnamaldehyde due to their polarity and ability to form hydrogen bonds with the compound.
What is the equation when you react acetone with phenyl hydrazine?
When acetone react with phenylhidrazine equation is phenylhidrazone of acetone, condensation product in which process water molecule eliminate.
What product would you expect if cinnamaldehyde and acetone reacts?
The reaction of cinnamaldehyde and acetone typically results in the formation of 2'-Hydroxychalcone, also known as butein. Butein is a natural chalcone derivative that has been studied for its various biological activities, including antioxidant and anti-inflammatory properties.
What is the mechanism for the aldol condesation reaction of acetone and p-anisaldehyde?
In the aldol condensation between acetone and p-anisaldehyde, the p-anisaldehyde first acts as the electrophile, accepting a proton to form an enolate ion. This enolate ion then attacks the carbonyl carbon of acetone, forming a new carbon-carbon bond. The resulting aldol product undergoes dehydration to form the final α,β-unsaturated ketone.
Would cinnamaldehyde react with bromine?
Yes, cinnamaldehyde can react with bromine to form dibromocinnamaldehyde. This reaction involves the addition of bromine across the carbon-carbon double bond in the cinnamaldehyde molecule.
What type of reaction is acetone reacted with triiodomethane?
An iodoform reaction is the type of reaction when acetone reacts with triiodomethane.
What is the solvents used to dissolve cinnamaldehyde?
Common solvents used to dissolve cinnamaldehyde include ethanol, acetone, and ethyl acetate. These solvents are effective in dissolving cinnamaldehyde due to their polarity and ability to form hydrogen bonds with the compound.
What is the equation when you react acetone with phenyl hydrazine?
When acetone react with phenylhidrazine equation is phenylhidrazone of acetone, condensation product in which process water molecule eliminate.
Why is the reaction between iodine and acetone catalysed?
The reaction between iodine and acetone is catalyzed by hydroxide ions present in the reaction mixture. The hydroxide ions help in the deprotonation of acetone, making it more reactive towards iodine. This catalysis increases the rate of reaction and allows for the formation of iodoform.
What is the reaction called when you dissolve styrofoam with acetone?
potato
Will baking soda neutralize acetone?
No, baking soda will not neutralize acetone. Acetone is a strong solvent and the chemical reaction between baking soda and acetone is not effective for neutralization. It is best to handle acetone with proper ventilation and safety precautions.
What is the chemical name of oil of cinnamon?
This oil is a mixture, not a compound; the principal component is cinnamaldehyde.
Chemical equation for the reaction of acetone and acidified potassium dichromate?
acetone does not react with potassium dichromate
Is cinnamaldehyde an aldehyde or ketone?
Cinnamaldehyde is an aldehyde. Its structure contains an aldehyde functional group (-CHO) attached to a benzene ring.
