Answer:
A student practicing for the outdoor track team begins to sweat. To what stimulus is the body responding?
Explanation:
Answer:
zero
Explanation:
I I think one should be so accurate with measurements and experiments
Hyperventilation<span> will blow off carbon dioxide which reduces the alkaline component of the </span>blood<span>, resulting in acidosis and a lower </span>blood pH<span>. (See Andromeda Strain). This is why re-breathing into a bag to increase carbon dioxide in your </span>blood will make you feel less faint. Basically <span>It increases the pH ... you can look at CO2 as an acid ... and when reduced ... alkalinization of the pH occurs</span>
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).
Answer:
NaOH is the limiting reactant.
Explanation:
Hello there!
In this case, since the reaction taking place between sodium hydroxide and chlorine has is:
Which must be balanced according to the law of conservation of mass:
Whereas there is a 2:1 mole ratio of NaOH to Cl2, which means that the moles of the former that are consumed by 0.85 moles of the latter are:
Therefore, since we just have 1.23 moles out of 1.70 moles of NaOH, we infer this is the limiting reactant.
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