Condensation polymerization involves the reaction of monomers with functional groups, resulting in the elimination of small molecules.

Addition polymerization involves the reaction of monomers with unsaturated bonds to form a polymer.

Condensation polymerization involves the elimination of a small molecule, such as water.

Hemoglobin is a transport protein that carries oxygen in the blood.

The quaternary structure of a protein is formed when two or more polypeptide chains assemble into a functional protein complex.

During alpha decay, helium nuclei (alpha particles) are emitted from the nucleus.

Beta decay involves the emission of beta particles, which are electrons or positrons.

Gamma radiation is the most penetrating type of radiation.

Alkanes typically undergo substitution reactions, especially with halogens.

Alkenes typically undergo addition reactions due to the presence of double bonds.

A condensation reaction occurs when two monosaccharides combine to form a disaccharide, releasing water.

A peptide bond is formed through a condensation reaction, where water is released.

Peptide bonds are formed through a condensation reaction, where a molecule of water is released.

Peptide bonds are formed through a condensation reaction between amino acids.

Dehydration synthesis is the reaction that links monomers together to form polymers by removing water.

Hydrogenation is the process of adding hydrogen to an alkene to convert it into an alkane.

The reaction CaCO3 → CaO + CO2 is a decomposition reaction, where one compound breaks down into two products.

The conversion of an alkene to an alkane is called hydrogenation, where hydrogen is added across the double bond.

The reaction is a nucleophilic substitution where the cyanide ion replaces the bromine atom.

The reaction between 1-bromopropane and sodium cyanide is a nucleophilic substitution reaction, resulting in the formation of propanenitrile.

The reaction of 1-bromopropane with sodium ethoxide is a nucleophilic substitution reaction where the ethoxide ion replaces the bromine atom.

When 1-chlorobutane is treated with aqueous KOH, a nucleophilic substitution reaction occurs, resulting in the formation of butanol.

The reaction of 1-chloropropane with aqueous KOH leads to nucleophilic substitution, resulting in the formation of propanol.

The reaction of 1-chloropropane with aqueous KOH leads to an elimination reaction, forming propene.

The reaction between 1-chloropropane and potassium cyanide is a nucleophilic substitution reaction, resulting in the formation of propanenitrile.

The reaction between 1-chloropropane and sodium cyanide is a nucleophilic substitution reaction where the cyanide ion replaces the chlorine atom.

The reaction is a nucleophilic substitution (S_N2) where iodide ion replaces the chlorine atom.

The treatment of 2-bromobutane with sodium ethoxide leads to an elimination reaction, forming an alkene.

The reaction of 2-bromopropane with aqueous KOH leads to an elimination reaction, forming propene.

The conversion of alkenes to alkanes involves the addition of hydrogen (hydrogenation).