Covalent bonds form when atoms share electrons. This sharing allows each atom to achieve its octet of electrons and greater stability. Methane, CH 4<span>, the simplest organic compound, contains covalent bonds. Carbon has four valence electrons, while hydrogen has one valence electron. By sharing these outer‐shell electrons, carbon and hydrogen complete their valence shells and become more stable. The duet of electrons on the hydrogen is isoelectronic with helium and forms a complete shell.</span>
Answer: Natural selection.
Explanation:
The natural selection is the process by which the organism that best suits the characters will survive and the organism which cannot adapt the changes will die.
The predators feed on their prey and the organism which hides easily in the environment due to its color is safe and the animals that cannot camouflage will die.
This is natural selection that more favored character is carried out over generations and other that cannot survive die.
Options :
The upward force is greater than the downward force.
The downward force is greater than the upward force.
The rightward force is greater than the leftward force.
The leftward force is greater than the rightward force.
Answer:
The downward force is greater than the upward force.
Explanation:
When the player jumps to dunk a basket ball, it requires an upward force exerted on the person due to the push by the person to jump, after dunking the basket ball, the player attains maximum height, where his final velocity becomes zero and his direction changes (from upward to downward), at this point his velocity increases due to the additional force exerted on the player due to the Earth's Gravitational pull - which is a downward force which acts on an object).
Hence, it could be concluded that the increase in speed of the basketball player as she returns to the ground means that the downward force is greater than the upward force acting on the player.
Answer:
The order of reactivity towards electrophilic susbtitution is shown below:
a. anisole > ethylbenzene>benzene>chlorobenzene>nitrobenzene
b. p-cresol>p-xylene>toluene>benzene
c.Phenol>propylbenzene>benzene>benzoic acid
d.p-chloromethylbenzene>p-methylnitrobenzene> 2-chloro-1-methyl-4-nitrobenzene> 1-methyl-2,4-dinitrobenzene
Explanation:
Electron donating groups favor the electrophilic substitution reactions at ortho and para positions of the benzene ring.
For example: -OH, -OCH3, -NH2, Alkyl groups favor electrophilic aromatic substitution in benzene.
The -I (negative inductive effect) groups, electron-withdrawing groups deactivate the benzene ring towards electrophilic aromatic substitution.
Examples: -NO2, -SO3H, halide groups, Carboxylic acid groups, carbonyl gropus.