Answer: The bond between a hydrogen atom and a sulfur atom is nonpolar covalent, so the electrons are shared.
Solution :
In the field of chemistry, the cationic polymerization is a kind of the chain growth polymerization where the cation initiator transfers the charge to the monomer and makes it more reactive. This kind of polymerization reaction is very sensitive to the temperature. With increase in temperature, the molecular weight as well as the reaction rate decreases rapidly.
Thus in the cationic polymerization of the 3,3-dimethyl-1-butene, the carbonation intermediate is formed and it rearranges itself. The attack o the 2nd alkene ca take place both the carbonations, so that random copolymer is formed.
When comparing single bonds between atoms of comparable types, the stronger the bond is, the bigger the atom, the weaker it is.
The length of the X-H bond lengthens while the strength of the bond shortens with increasing halogen size (F-H strongest, I-H weakest). When comparing single bonds between atoms of similar sorts, the larger the atom, the weaker the bond. It can be explained by the fact that less energy is required to break the bond the bigger the atom's atomic size. The force of attraction from the nucleus to the outermost orbit will be less for iodine since it has a larger atom than the other elements in the group.
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The safety feature aimed at keeping nuclear radiation contained is steel-reinforced concrete.
<h3>What is nuclear power plant?</h3>
A nuclear power plant is a building with reactors that contain controlled nuclear reactions to produce energy.
Nuclear power plants are able to generate warm water by using atomic properties of matter (i.e.,m the process of nuclear fission), which is in turn converted into steam to move turbines.
The walls of nuclear power reactors are composed of steel-reinforced concrete in order to avoid radiation release.
In conclusion, the safety standard property that maintains nuclear radiation contained is steel-reinforced concrete.
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Answer:
True
Explanation:
Aromatic compounds undergo substitution rather than addition reactions because the aromatic structure is maintained.
Electrophilic aromatic substitution begins with attack of the electrophile on the aromatic ring to yield a delocalized intermediate called the arenium intermediate. Loss of hydrogen from this intermediate yields the final product.
