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.
Answer:
The elements in each group have the same number of electrons in the outer orbital. Those outer electrons are also called valence electrons.
Explanation:
It creates chlorofluorocarbons(CFCs) also would create biooxygen but in the multiple choice it only shows the CFCs
Answer:
Nitrogen
Oxygen
Argon
Carbon Dioxide
Methane
Ozone
Explanation:
N₂ accounts for 78% of the atmosphere.
O₂ accounts for 21% of the atmosphere.
Ar accounts for 0.9% of the atmosphere.
CO₂, CH₄, and O₃ only take up 0.1% of the atmosphere.