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 air pressure. the air pressure increases as the altitude an object is at increases.
Answer: any answer choices
Explanation:
Answer:
Charge= -2.
Gains two electron into the 4p^4 to become 4p^6.
Explanation:
The element in the periodic table/chart that matches with the valence electron configuration is Selenium with full electron configuration of [Ar] 3d^10 4s^2 4P^4 which is a non-metal that is found in group 4 of the periodic table/chart.
Selenium can receive 2 more electrons on the 4p^4 to give a -2(minus 2) ion that is Se^2-.
Selenium can also loose 2 electron from 4s^2 to give a +2 ion that is Se^2+.
Selenium can also loose 2 electrons from 4s^2 and 2 electrons from 4p^4 to form Se^4+.
Selenium can also loose 2 electrons from 4s^2 and 4 electrons from 4p^4 to form Se^6+.
Thus, in order to form a monatomic ion with a charge(we will be making use of the most stable one). Thus, it will gain two more electron since this is easier to become 4s^2 4p^6.
