Answer:
The glycosylation reaction or glycoside formation is an organic reaction in which the hemiacetal group of cyclists ketoses or aldoses turns into acetals, named glycosides. Reaction in the attached picture.
Explanation:
Carbohydrates can be found in an open-chain form or a cyclic form. For the second one, the carbonyl group of the aldehyde could react with the alcohol group of the molecule to form the cycle. As shown in the attached picture, the alcohol group of this cyclic form could react with an alcohol (like methanol) in acidic conditions to form an acetal. These compounds are stable at neutral and acidic conditions, but they hydrolyze at basic conditions. This reaction produces both acetals anomers (α and β) because the attack of the nucleophile (alcohol) could be from both sides. However, the most stable anomer will predominate.
The correct answers are :
Changing the volume of the system.
Changing the temperature of the system.
Equilibrium will remain unaffected if the concentration of products and reactants are kept the same, and the temperature of the system is kept constant.
As the system is closed, we cannot add or remove products or reactants.
Change in temperature will shift the chemical equilibrium towards the reactant or product depending on whether the reaction is exothermic or endothermic.
Also change in volume will shift the chemical equilibrium of a chemical reaction if the reactants or products or both are gases.
This is categorized as a combustion reaction.
Salt dissolving in a glass of water, using electricity to break down water into hydrogen and oxygen, rust forming on an iron fence and gas burning on a stove.