Answer:
Total volume after adding crystal = 26.7 mL
Explanation:
Given data:
Density of crystal = 2.65 g/mL
Mass of sample = 4.46 g
Volume of water = 25.0 mL
Volume after adding crystal = ?
Solution:
First of all we will calculate the volume of crystal.
d = m/v
2.65 g/mL = 4.46 g/ v
v = 4.46 g/2.65 g/mL
v = 1.7 mL
Total volume after adding crystal = Volume of water + Volume of metal
Total volume after adding crystal = 25.0 mL + 1.7 mL
Total volume after adding crystal = 26.7 mL
NH4I (aq) + KOH (aq) in chemical equation gives
NH4I (aq) + KOH (aq) = KI (aq) + H2O(l) + NH3 (l)
Ki is in aqueous state H2o is in liquid state while NH3 is in liquid state
from the equation above 1 mole of NH4I (aq) react with 1 mole of KOH(aq) to form 1mole of KI(aq) , 1mole of H2O(l) and 1 Mole of NH3(l)
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).