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Reaction of camphor with an aromatic amine can be achieved using 10% zinc chloride as a catalyst in a suitable organic solvent under reflux conditions.
See "Preparation and reduction of camphor imines" - Bolton, Danks & Paul. Dept of Chem, University of Surrey, 1994.
The abstract of the paper does not identify which solvent is used, reflux time or product yield.
What else can I help you with?
Is schiff base is prepared by mannich reaction?
No, Schiff base is not prepared by Mannich reaction. Schiff base is typically formed through the condensation reaction between a primary amine and a carbonyl compound. Mannich reaction, on the other hand, involves the condensation of a primary or secondary amine, a carbonyl compound, and formaldehyde or a derivative.
Why glucose is used for the preparation of schiff base?
Glucose is used for the preparation of Schiff base because it contains multiple hydroxyl groups that can react with an aldehyde or ketone to form a Schiff base. The reaction between glucose and the carbonyl compound leads to the formation of a stable imine or Schiff base linkage.
What is the mechanism of schiff base formation?
Schiff base formation involves the nucleophilic addition of a primary amine to a carbonyl group (aldehyde or ketone), resulting in the formation of an imine intermediate. The imine intermediate then undergoes a proton transfer to form the final Schiff base compound, which is characterized by a C=N bond. This reaction is reversible and can be catalyzed by acid or base.
Equation of formaldehyde schiff's reagent benzaldehyde schiff's reagent and acetone schiff's reagent?
Formaldehyde Schiff's reagent: It is a solution of formaldehyde and sulfuric acid, used to detect the presence of aldehydes. The equation involves the formation of a colored compound with aldehydes. Benzaldehyde Schiff's reagent: Benzaldehyde can act as a Schiff's base with primary amines to form imines. The reaction results in the formation of a colored compound. Acetone Schiff's reagent: Acetone can react with a primary amine to form a Schiff's base, leading to the formation of a colored compound.
Schiff base reaction terms and conditions?
The Schiff base reaction involves the condensation of an amine with an aldehyde or ketone to form a carbon-nitrogen double bond. It typically occurs in a solvent such as ethanol or methanol under mild acidic or basic conditions. The reaction is reversible, and the conditions must be chosen carefully to favor the formation of the desired product.
Is schiff base is prepared by mannich reaction?
No, Schiff base is not prepared by Mannich reaction. Schiff base is typically formed through the condensation reaction between a primary amine and a carbonyl compound. Mannich reaction, on the other hand, involves the condensation of a primary or secondary amine, a carbonyl compound, and formaldehyde or a derivative.
Why glucose is used for the preparation of schiff base?
Glucose is used for the preparation of Schiff base because it contains multiple hydroxyl groups that can react with an aldehyde or ketone to form a Schiff base. The reaction between glucose and the carbonyl compound leads to the formation of a stable imine or Schiff base linkage.
What is the mechanism of schiff base formation?
Schiff base formation involves the nucleophilic addition of a primary amine to a carbonyl group (aldehyde or ketone), resulting in the formation of an imine intermediate. The imine intermediate then undergoes a proton transfer to form the final Schiff base compound, which is characterized by a C=N bond. This reaction is reversible and can be catalyzed by acid or base.
Equation of formaldehyde schiff's reagent benzaldehyde schiff's reagent and acetone schiff's reagent?
Formaldehyde Schiff's reagent: It is a solution of formaldehyde and sulfuric acid, used to detect the presence of aldehydes. The equation involves the formation of a colored compound with aldehydes. Benzaldehyde Schiff's reagent: Benzaldehyde can act as a Schiff's base with primary amines to form imines. The reaction results in the formation of a colored compound. Acetone Schiff's reagent: Acetone can react with a primary amine to form a Schiff's base, leading to the formation of a colored compound.
Why schiff base is so called?
hi, schiff base is so called because Hugo schiff was discover it
How schiff's base was discovered?
Schiff base was proposed by Hugo Schiff and are imines that are formed by the condensation of aldehydes or ketones with primary amines.
Schiff base reaction terms and conditions?
The Schiff base reaction involves the condensation of an amine with an aldehyde or ketone to form a carbon-nitrogen double bond. It typically occurs in a solvent such as ethanol or methanol under mild acidic or basic conditions. The reaction is reversible, and the conditions must be chosen carefully to favor the formation of the desired product.
What is the chemical reaction for furfural and a primary aromatic amine C5H4O2 plus Nh2?
What is the chemical reaction for furfural and a primary aromatic amine C5H4O2 plus Nh2?y
Dimethyl amine is stronger base than methyl amine?
How am I suppose to know huh
How Schiff base discovered by accidentally or by research?
Hugo german scientist
Is tributyl amine is basic?
Yes, tributylamine is a weak base due to the presence of the amine group that can accept protons. It is commonly used as a base in organic chemistry reactions.
Is camphor an acid or a base?
IIIIt is a slightly acid having ph of 5.5 to 6.5
