B is correct. As you move down group 1, the elements become more reactive with other elements because the electrons have a weaker attraction to their own atoms nucleus which means attraction with other elements is much stronger, making the atom more reactive.
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).
C5H12 + 8 O2 → 5 CO2 + 6 H2O
8 molecules of O2 are required.
Answer:
Explanation:
For a chemical reaction, the enthalpy of reaction (ΔHrxn) is … ... to increase the temperature of 1 g of a substance by 1°C; its units are thus J/(g•°C). ... Both Equations 12.3.7 and 12.3.8 are under constant pressure (which ... The specific heat of water is 4.184 J/g °C (Table 12.3.1), so to heat 1 g of water by 1 ..
Answer:
Explanation:
Hello,
In this case, we apply the Gay-Lussac's law which allows us to understand the pressure-temperature behavior as a directly proportional relationship:
Thus, we solve for the final pressure P2 to obtain it as shown below:
Hence, we notice that the temperature doubles as well as the pressure.
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