For better representation, let me rewrite the electronic configuration:
<span>1s</span>²<span>2s</span>²<span>2p</span>⁶<span>3s</span>²<span>3p</span>⁶<span>4s</span>²<span>3d</span>⁴
The exponents represent the number of electrons in the designated subshell. Thus, the total number of electrons are:
# of electrons = 2+2+6+2+6+2+4 = 24
Assuming this is in neutral state, the element with an atomic number of 24 is Chromium. Thus, the answer is Cr.
Answer:
<h2>2 g/mL</h2>
Explanation:
The density of a substance can be found by using the formula
From the question we have
We have the final answer as
<h3>2 g/mL</h3>
Hope this helps you
Answer:
The correct formula for tetraphosphorous octaoxide is P₂O₅
Natural gas is primarily composed of methane (CH4)
Natural gas is a naturally occurring hydrocarbon mixture which is primarily composed of Methane(CH4), but it also contains ethane,propane and heavier hydrocarbon. In addition it contain small amount of nitrogen, carbon dioxide,hydrogen sulfide and traces amount of water.
Answer:
a. electrophilic aromatic substitution
b. nucleophilic aromatic substitution
c. nucleophilic aromatic substitution
d. electrophilic aromatic substitution
e. nucleophilic aromatic substitution
f. electrophilic aromatic substitution
Explanation:
Electrophilic aromatic substitution is a type of chemical reaction where a hydrogen atom or a functional group that is attached to the aromatic ring is replaced by an electrophile. Electrophilic aromatic substitutions can be classified into five classes: 1-Halogenation: is the replacement of one or more hydrogen (H) atoms in an organic compound by a halogen such as, for example, bromine (bromination), chlorine (chlorination), etc; 2- Nitration: the replacement of H with a nitrate group (NO2); 3-Sulfonation: the replacement of H with a bisulfite (SO3H); 4-Friedel-CraftsAlkylation: the replacement of H with an alkyl group (R), and 5-Friedel-Crafts Acylation: the replacement of H with an acyl group (RCO). For example, the Benzene undergoes electrophilic substitution to produce a wide range of chemical compounds (chlorobenzene, nitrobenzene, benzene sulfonic acid, etc).
A nucleophilic aromatic substitution is a type of chemical reaction where an electron-rich nucleophile displaces a leaving group (for example, a halide on the aromatic ring). There are six types of nucleophilic substitution mechanisms: 1-the SNAr (addition-elimination) mechanism, whose name is due to the Hughes-Ingold symbol ''SN' and a unimolecular mechanism; 2-the SN1 reaction that produces diazonium salts 3-the benzyne mechanism that produce highly reactive species (including benzyne) derived from the aromatic ring by the replacement of two substituents; 4-the free radical SRN1 mechanism where a substituent on the aromatic ring is displaced by a nucleophile with the formation of intermediary free radical species; 5-the ANRORC (Addition of the Nucleophile, Ring Opening, and Ring Closure) mechanism, involved in reactions of metal amide nucleophiles and substituted pyrimidines; and 6-the Vicarious nucleophilic substitution, where a nucleophile displaces an H atom on the aromatic ring but without leaving groups (such as, for example, halogen substituents).
