benzoic acid + Sodium Hydroxide ==> water + sodium benzoate
Since in this case the alanine will behave as a base, the equation will be: CH3CH(NH2)COOH + HCl -> H2O + CH3CH(NH2)COCl As it's a neutralisation reaction (products must be water and a salt).
Ethanoic acid can be converted into methenamine by reacting it with formaldehyde in the presence of aqueous ammonia. This reaction undergoes a condensation reaction to form methenamine as the final product.
No, substances containing the -NH2 group are basic. The NH2- ion is extremely basic.
Anthranilic acid + ethanol amine C6H4(NH2)COOH + OHCH2CH2NH2 = C6H4(NH2)COOCH2CH2NH2 + H2O Sulphuric acid(H2SO4) is an acid catalyst which deprotonates the carboxylic group(COOH) of anthranilic acid and removes the hydroxy(OH) group from ethanol amine. The (H+) proton then attaches to the (-OH) to form water(H2O) as a byproduct. The deprotonated carboylate(COO-) group of anthranilic acid then attaches to the the (+CH2CH2NH2) to form the amide/ester product. The structure is amine (NH2 bonded to benzene ring) with (COOCH2CH2NH2) bonded to the ortho position of the benzene ring
No, urea phosphate is a compound formed from urea and phosphoric acid, while uric acid is a product of the metabolic breakdown of purines in the body. Urea phosphate is commonly used as a fertilizer, while uric acid is a waste product that is excreted from the body through urine.
Since in this case the alanine will behave as a base, the equation will be: CH3CH(NH2)COOH + HCl -> H2O + CH3CH(NH2)COCl As it's a neutralisation reaction (products must be water and a salt).
Ethanoic acid can be converted into methenamine by reacting it with formaldehyde in the presence of aqueous ammonia. This reaction undergoes a condensation reaction to form methenamine as the final product.
No, substances containing the -NH2 group are basic. The NH2- ion is extremely basic.
NH2
Anthranilic acid + ethanol amine C6H4(NH2)COOH + OHCH2CH2NH2 = C6H4(NH2)COOCH2CH2NH2 + H2O Sulphuric acid(H2SO4) is an acid catalyst which deprotonates the carboxylic group(COOH) of anthranilic acid and removes the hydroxy(OH) group from ethanol amine. The (H+) proton then attaches to the (-OH) to form water(H2O) as a byproduct. The deprotonated carboylate(COO-) group of anthranilic acid then attaches to the the (+CH2CH2NH2) to form the amide/ester product. The structure is amine (NH2 bonded to benzene ring) with (COOCH2CH2NH2) bonded to the ortho position of the benzene ring
Toluene + HNO3/H2SO4 --> p-nitrotoluene (para directed nitration) p-nitrotoluene + Zn/HCl --> p-aminotoluene (changing NO2 to NH2 by reduction) p-aminotoluene +Br2 --> bromination ortho to NH2 Remove NH2 via diazonium salt and decomposition with 1) HONO (which is NaNO2+HCl), 2) H3PO2 for the final product.
NH2=amino group COOH=Carboxylic acid therefore -oic acid
NH2-COOH is the chemical formula of the hypothetical carbamic acid. This group exist in aminoacids, carbamates, urethanes etc.
No, urea phosphate is a compound formed from urea and phosphoric acid, while uric acid is a product of the metabolic breakdown of purines in the body. Urea phosphate is commonly used as a fertilizer, while uric acid is a waste product that is excreted from the body through urine.
No, formic acid is not a simple amino acid. It is a simple carboxylic acid with the chemical formula HCOOH. Amino acids are organic compounds containing an amino group (-NH2) and a carboxyl group (-COOH).
The general formula of an amino acid is R-CH(NH2)-COOH, where R represents the side chain specific to each amino acid. This formula represents the basic structure common to all amino acids, which includes an amino group (-NH2) and a carboxyl group (-COOH) bonded to a central carbon atom.
The functional groups of an amino acid are the amino group (-NH2) and the carboxyl group (-COOH).