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Does Ares have amines?
Amines being organic compounds and functional groups that contain a basic nitrogen atom with a lone pair.Probably not something the Greek god of war would be interested in.
What are four types of basic organic macromolecules and how are they important in the body?
carbohydrates,amines,lipids,fats.
Would water be a suiable solvent for every dye?
-Cationic dyes (basic dyes) are soluble in polar solvents such as water, alcohols -Nonionic Fat-soluble dyes line metal-free azo and anthraquinone dyes are soluble in aromatic and aliphatic hydrocarbons. -Metal-complex dyes are normally soluble in alcohols, ketones, glycoethers
Is aniline yellow a basic dye?
Yes, it is basic in the chemical sense because it contains the amine group -NH2 which can accept a proton.
Why amine is soluble in acid?
they have a lone pair of electrons which allows them to attract protons , so they are basic in nature
Dimethyl benzyl amine is a ionic compound?
It is slightly basic (as amines are) but it is neutral and not ionic (Cf. NH3)
What is difference between amine and amide?
An Amine is best defined as a derivative of ammonia (NH3) where one or more N-H bonds are replaced by N-C bonds. Primary amines have one N-H bond replaced by a N-c bond, whereas secondary has two N-C bonds with one N-H bond and tertiary has all three N-C bonds making the molecular formula NC3. An amide is a nitrogen bonded to a carbonyl group.
Amides are less basic than amines because?
Because in amines (R-NH2),nitrogen have lone pair of electrons which serves to accept proton thatswhy it is basic,while in amides (RCO-NH2) the amine group bonded with cabonyl group and due to high electronegetivity of oxygen NH2 group involve in resonance thats why it is less basic than amines.
Is tributyl amine is basic?
yes. it is basic
Do amines tend to be acid neutral or basic?
Amines are basic due to the presence of lone pair of electrons on Nitrogen atom they may accept a proton from an acid.
Among benzyl amine aniline acetanilide and p-nitro aniline which is the most basic compound?
benzyl amine is the most basic
Why do amines act as bases?
in amines a unshared pare of electron is present over nitrogen which is responsible for its basic character.
What is the polarity of caffeine?
caffeine is polar due to the amines group and it is basic
What is the pH of ethyl amine would be?
Ethylamine solution is basic.
How do you do diazotization titration?
The process by which an aromatic primary amine is converted to a diazonium compound. The preparation and reactions of diazonium salts were discovered in 1858 and were the basis of the synthetic dye industry and the development of other industrial chemistry in Europe. In diazotization, sodium nitrite is added to a solution of the amine in aqueous acid solution at 0–5°C (32–41°F). Reaction of the amine with nitrous acid gives a nitrosamine. Tautomerization and loss of water lead to the diazonium ion, which is stabilized by delocalization of the positive charge at the ortho and para carbon atoms of the ring, as in the reaction below. See also Amine; Aromatic hydrocarbon; Delocalization. The overall reaction is simple and very general. Substituents of all types—alkyl, halogen, nitro, hydroxyl, sulfonic acid—can be present at any position. Heterocyclic amines such as aminothiazole or aminopyridines can also be diazotized. Aromatic diamines are converted to bis-diazonium compounds. Diazonium salts are generally used and handled in aqueous solution; they are explosive if isolated and dried. The great importance of diazonium compounds in dye technology lies in the coupling reactions that occur with an activated aromatic ring, such as that in phenols or aromatic amines. Coupling, or electrophilic substitution by ArN2+, gives compounds with an arylazo group at the position para or ortho to OH or NH2. Reaction with amines occurs in weak acid solution. With phenols the phenoxide ion is the reactive species, and slightly basic solution is used. See also Chemical equilibrium. The azo dyes obtained in these coupling reactions are one of the important types of synthetic dyes. The color of the dye can be varied widely by choice of diazonium and coupling components. The coupling reaction lends itself to an important method of applying the dye to fabrics. In this process the coupling reagent, such as a naphtholsulfonic acid, is absorbed onto the fiber, and the coupling reaction is then carried out directly on the fiber by passing the fabric through a bath of the diazonium solution. See also Dye.
How do you do diazotization?
The process by which an aromatic primary amine is converted to a diazonium compound. The preparation and reactions of diazonium salts were discovered in 1858 and were the basis of the synthetic dye industry and the development of other industrial chemistry in Europe. In diazotization, sodium nitrite is added to a solution of the amine in aqueous acid solution at 0–5°C (32–41°F). Reaction of the amine with nitrous acid gives a nitrosamine. Tautomerization and loss of water lead to the diazonium ion, which is stabilized by delocalization of the positive charge at the ortho and para carbon atoms of the ring, as in the reaction below. See also Amine; Aromatic hydrocarbon; Delocalization. The overall reaction is simple and very general. Substituents of all types—alkyl, halogen, nitro, hydroxyl, sulfonic acid—can be present at any position. Heterocyclic amines such as aminothiazole or aminopyridines can also be diazotized. Aromatic diamines are converted to bis-diazonium compounds. Diazonium salts are generally used and handled in aqueous solution; they are explosive if isolated and dried. The great importance of diazonium compounds in dye technology lies in the coupling reactions that occur with an activated aromatic ring, such as that in phenols or aromatic amines. Coupling, or electrophilic substitution by ArN2+, gives compounds with an arylazo group at the position para or ortho to OH or NH2. Reaction with amines occurs in weak acid solution. With phenols the phenoxide ion is the reactive species, and slightly basic solution is used. See also Chemical equilibrium. The azo dyes obtained in these coupling reactions are one of the important types of synthetic dyes. The color of the dye can be varied widely by choice of diazonium and coupling components. The coupling reaction lends itself to an important method of applying the dye to fabrics. In this process the coupling reagent, such as a naphtholsulfonic acid, is absorbed onto the fiber, and the coupling reaction is then carried out directly on the fiber by passing the fabric through a bath of the diazonium solution. See also Dye.
What Mechanism involved in Philips condensation reaction?
is a condensation reaction in which an amines are allowed to react with acids to form amides.first amine react with acid and form an amide.again formed amide reacts with an acid to form an second amide called benzimidazole[which has similar structure of benzene] it has basic nucleus of imidazole
