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.
V2 = 250 ml
Explanation:
Given:
P1 = 0.99 atm. V1 = 240 ml
P2 = 0.951 atm. V2 = ?
We can use Boyle's law to solve for V2
P1V1 = P2V2
V2 = (P1/P2)V1
= (0.99 atm/0.951 atm)(240 ml)
= 250. ml
Increasing order of strength needed to break bonds:
temporary dipole induced dipole interactions
Permanent dipole induced dipole interactions
Hydrogen bonding