Because the h2o level rises
hydrolysis
Unsymmetrical addition reaction is a chemical reaction in which two different reactants add to an unsymmetrical molecule, resulting in the formation of a new molecule with different substituents at the reacting sites. This type of reaction typically occurs with alkenes or alkynes and can lead to the formation of stereoisomers when chiral compounds are involved. Examples include the addition of hydrogen halides to alkenes or the addition of nucleophiles to carbonyl compounds.
As substrate concentration increases, the initial reaction rate generally increases as well, due to a higher likelihood of substrate molecules colliding with enzyme active sites. However, this increase continues only until a certain point, known as the saturation point, where all active sites of the enzyme are occupied. Beyond this saturation point, further increases in substrate concentration do not significantly affect the reaction rate, as the enzymes are already working at their maximum capacity.
Compounds with multiple bonds, such as alkenes and alkynes, typically take part in addition reactions. In these reactions, the multiple bond is broken and new atoms or groups are added to the molecule.
In this type of polymerization monomers are added successive without any loss of molecule or atom.
Because the h2o level rises
An addition reaction is a chemical reaction in which two or more reactants combine to form a single product. This type of reaction typically involves the addition of atoms or groups to a double or triple bond in a molecule.
An addition reaction is when 1 molecule combines with another molecule and becomes 1 bigger molecule. There are no other products in this process; just the 2 molecules.
hydrolysis
Unsymmetrical addition reaction is a chemical reaction in which two different reactants add to an unsymmetrical molecule, resulting in the formation of a new molecule with different substituents at the reacting sites. This type of reaction typically occurs with alkenes or alkynes and can lead to the formation of stereoisomers when chiral compounds are involved. Examples include the addition of hydrogen halides to alkenes or the addition of nucleophiles to carbonyl compounds.
... addition reaction; the hydrogen molecule is split, one of its atoms is added to each carbon atom that is initially double bonded, and an alkene becomes an alkane. --- ... known as hydrogenation.
The reverse reaction of a condensation reaction would be a hydrolysis reaction. In a condensation reaction, two molecules combine to form a larger molecule with the loss of a smaller molecule such as water. In a hydrolysis reaction, a larger molecule is broken down into smaller molecules through the addition of water.
In organic chemistry, an activator is a molecule that increases the rate of a chemical reaction, while a deactivator is a molecule that decreases the rate of a chemical reaction.
With out heat only a certain amount of solute is able to go into solution. With the addition of heat (now an endothermic reaction) more solute will be forced into solution creating a supersaturated solution.
The product of ethene's reaction with chlorine is 1,2-dichloroethane. This reaction involves the addition of a chlorine atom to each carbon atom in the ethene molecule.
Compounds with multiple bonds, such as alkenes and alkynes, typically take part in addition reactions. In these reactions, the multiple bond is broken and new atoms or groups are added to the molecule.
A molecule that speeds up a chemical reaction is called a catalyst. Catalysts work by reducing the activation energy needed for a reaction to occur, which increases the rate of the reaction without being consumed in the process.