Answer:
Hartwell's yeast
Explanation: A model organism for studying somatic mutations and cancer."
Answer:
cheese and bread
Explanation:
2 bread 1 cheese = cheese sandwich
We can exemplify with H2O (water)
H= nonmetalic
O= Nonmetalic
A bond with nonmetalic and nonmetalic is covalent bond.
Hope it helps!!
#MissionExam001
Stereochemistry, a subdiscipline of chemistry, involves the study of the relative spatial arrangement of atoms that form the structure of molecules and their manipulation.
<h3>What is the use of stereochemistry?</h3>
Using stereochemistry, chemists can work out the relationships between different molecules that are made up from the same atoms. They can also study the effect on the physical or biological properties these relationships give molecules.
<h3>Why is it called stereochemistry?</h3>
The term “stereochemistry” is derived from the Greek “stereos” meaning solid—it refers to chemistry in three dimensions. Since nearly all organic molecules are three dimensional (with the exception of some olefins and aromatics to be discussed later), stereochemistry cannot be considered a branch of chemistry.
Learn more about stereochemistry here:
<h3>
brainly.com/question/13266152</h3><h3 /><h3>#SPJ4</h3>
Answer:
Nitrobenzene < Bromobenzene < Benzene < Phenol
Explanation:
Aromatic compounds undergo electrophilic aromatic substitution reaction in the presence of relevant electrophiles. Certain substituents tend to increase or decrease the tendency of an aromatic compound towards electrophilic aromatic substitution reaction.
Substituents that increase the electron density around the ring such as in phenol tends to make the ring more reactive towards electrophilic substitution. Halogens such as bromine has a -I inductive effect as well as a +M mesomeric effect.
However the -I(electron withdrawing effect) of the halogens supersedes the +M electron donation due to mesomeric effect.
Putting all these together, the order of increasing reactivity of the compounds towards electrophilic aromatic substitution is;
Nitrobenzene < Bromobenzene < Benzene < Phenol