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.
A substance can dissolve in another when they have thee same type of intermolecular interaction.
<h3>What is solubility?</h3>
The term solubility of a solute refers to the extent to which a solute dissolve in a solvent. We must know that a substance can dissolve in another when they have thee same type of intermolecular interaction.
Thus;
a) Octane (C8H18) mixes well with CCl4 because they are both non polar substances.
b) Methanol (CH3OH) is mixed with water in all ratios because the both are polar substances.
c) NaBr dissolves very poorly in acetone (CH3 ― CO ― CH3) because acetone is only slightly polar.
Learn more about solubility:brainly.com/question/8591226
#SPJ1
Answer:
Plants using glucose to make ATP molecules during the process of photosynthesis which results in the plant releasing oxygen.
This is cellular respiration. ↑
Answer:
endothermic
Explanation:
the negative sign of the heat indicates that heat is being drawn into the system, thus endothermic