The correct answer to the question that is being presented above would be letter c. change in particle size. Changes in pressure, temperature, and concentration are stressors that cause change in chemical equilibrium.
Glucose is the major example of monosacchrides
succrose is an example of disaccharide
and both starch and cellulose are examples of polysaccharides
hope that helps :)
Done with an experiement and if he has enough data he can compare it and make his results more accurate please make me brainliest
Answer:
The system gains 126100 J
Explanation:
The heat can be calculated by the equation:
Q = nxCxΔT, where Q is the heat, C is the heat capacity,n is the number of moles and ΔT is the variation of temperature (final - initial). The number of moles is the mass divided by the molar mass, so:
n = 250/4 = 62.5 mol.
The system must be in thermal equilibrium with the surroundings, so if the temperature of the surroundings decreased 97 K, the temperature of the system increased by 97 K, so ΔT = 97 K
Q = 62.5x20.8x97
Q = 126100 J
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).
