A carboxylic acid and an amine react to form nylon.
The functional groups of a molecule, such as hydroxyl (-OH), carbonyl (C=O), amino (-NH2), or carboxyl (-COOH) groups, are most likely to react with other molecules due to their high reactivity. These functional groups can participate in various chemical reactions to form new bonds with other molecules.
Beta carotene contains two functional groups: a system of conjugated double bonds that form a polyene chain and two cyclic structures at each end of the chain. These functional groups are responsible for beta carotene's color and its role as a precursor for vitamin A in the body.
Nylon 6,6 polymer forms at the interface of two liquid phases because the two reactants required for its formation are present at the interface, promoting polymerization. The reactants are sebacoyl chloride and hexamethylene diamine, which react to form nylon 6,6 polymer at the liquid-liquid interface due to the localized high concentration of reactants.
The noun form of the adjective functional is functionality.The word functional is the adjective form of the noun function.
Bromine in chloroform typically tests for the presence of alkenes or aromatic compounds. Bromine will react with the double bond or aromatic ring to form a dibromo compound, resulting in a color change from red-brown to colorless. This test is commonly known as the bromine test.
Polyesters are commonly made from an organic alcohol (containing hydroxyl [OH] groups) and a carboxylic acid (containing carboxyl [COOH] groups).
The pair of functional groups that can be part of a condensation reaction to form a polymer chain is hydroxyl (-OH) and carboxyl (-COOH) groups. The hydroxyl group provides the -OH to form water during the condensation reaction, linking monomers together to form the polymer chain.
The functional groups of a molecule, such as hydroxyl (-OH), carbonyl (C=O), amino (-NH2), or carboxyl (-COOH) groups, are most likely to react with other molecules due to their high reactivity. These functional groups can participate in various chemical reactions to form new bonds with other molecules.
6-aminohexanoic acid contains two functional groups, an amine group and a carboxylic acid group, that can react with each other. When these functional groups react, they form amide linkages, resulting in the formation of a polymer through a process known as polyamide synthesis.
Condensation polymerization occurs when two monomers react to form a polymer, with a small molecule (often water) being produced as a byproduct. The reaction typically requires high temperatures and longer reaction times compared to addition polymerization, as well as the presence of functional groups (such as hydroxyl or carboxyl groups) on the monomers that can react to form covalent bonds.
Because of free rotation of one phenyl group w r to the other thus it unable to form picrate
Beta carotene contains two functional groups: a system of conjugated double bonds that form a polyene chain and two cyclic structures at each end of the chain. These functional groups are responsible for beta carotene's color and its role as a precursor for vitamin A in the body.
The functional group involved in forming disulfide bonds is the sulfhydryl group, which consists of a sulfur atom bonded to a hydrogen atom (-SH). In proteins, two sulfhydryl groups from cysteine amino acids can undergo a redox reaction to form a covalent bond called a disulfide bond (-S-S-), stabilizing the protein's structure.
I think it's because the covalent bonds are strong, and therefore unreactive to acids & alkalis. You'd need to get alkanes in gas form to make it react, but you'd still need energy for it to react, like, say, heat perhaps?
Nylon 6,6 polymer forms at the interface of two liquid phases because the two reactants required for its formation are present at the interface, promoting polymerization. The reactants are sebacoyl chloride and hexamethylene diamine, which react to form nylon 6,6 polymer at the liquid-liquid interface due to the localized high concentration of reactants.
Both carbon skeletons and functional groups put together, add, or have atomos of oxygen, hydrogen, and carbon. Different arrangements of atoms bonded to a carbon skeleton can form functional groups, wich give specific properties to molecules.
The two functional side groups included in the straight-chain form of all monosaccharides are hydroxyl groups (-OH) and carbonyl groups (C=O). The hydroxyl groups can be found on the carbon atoms, while the carbonyl group is typically located at either end of the carbon chain, forming an aldehyde (-CHO) in aldoses or a ketone (C=O) in ketoses.