Organisms within each group are then further divided into smaller groups. These smaller groups are based on more detailed similarities within each larger group. This grouping system makes it easier for scientists to study certain groups of organisms.
It's Synthesis, single replacement is incorrect.
c. a tertiary alcohol; when a ketone reacts with a grignard reagent followed by protonation a tertiary alcohol is formed.
More about tertiary alcohol:
No hydrogen atoms are bonded to the functional group's carbon in a tertiary alcohol. Alcohols that have a hydroxyl group bonded to the carbon atom and are linked to three alkyl groups are referred to as tertiary alcohols. These alcohols' structural makeup largely determines their physical characteristics.
This -OH group's existence enables alcohols to create hydrogen bonds with the atoms next to them. Because of this weak connection, alcohols have higher boiling points than their alkane counterparts.
The alcohol is referred to as a tertiary (3°) alcohol if the carbon atom carrying the alcohol group is connected to three other carbon atoms in the alcohol molecule.
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Answer:
The addition of sulfate ions shifts equilibrium to the left.
Explanation:
Hello!
In this case, according to the following ionization of strontium sulfate:

It is evidenced that when sodium sulfate is added, sulfate,
is actually added in to the solution, which causes the equilibrium to shift leftwards according to the Le Ch athelier's principle. Thus, the answer in this case would be:
The addition of sulfate ions shifts equilibrium to the left.
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