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.
I think B or D because an eye obviously doesn't have a lense, mirror..maybe sorry for not giving u straight forward response
Answer:
Electronegativity varies in a predictable way across the periodic table. Electronegativity increases from bottom to top in groups, and increases from left to right across periods. Thus, fluorine is the most electronegative element, while francium is one of the least electronegative.Explanation:
Fe3N2, also known as Iron (II) nitride, is an ionic compound.
Ionic compounds are compounds that consists of metals and non-metals bonded with ionic bonds. The metal ion gives up electron(s) to the non-metals.
Since iron is a metal and nitrogen is an non-metal, the bond they would form would be an ionic bond. Iron gives up 2 electrons to form iron(II) ion, while nitrogen gains 3 electrons to form nitride ion. Since one iron cannot let a nitrogen gain 3 electrons, so in the compound, there would be 3 iron (ii) ions that has given up 6 electrons in total while 2 nitride ions have gained 6 electrons in total.