Answer:
4.5 kilograms of silicon dioxide is required to produce 3.00 kg of SiC.
Explanation:
The balanced equation for the reaction between silicon dioxide and carbon at high temperature is given as:
1 mole silicon dioxide reacts with 3 moles of carbon to give 1 moles of silicon carbide and 2 moles of carbon monoxide.
Mass of SiC = 3.00kg = 3000.00 g
1 kg = 1000 g
Molecular mass of SiC = 40 g/mol
Moles of SiC = 
According to reaction, 1 mole of SiC is produced from 1 mole of silicon dioxide.
Then 75 moles of SiC will be produce from:
of silicon dioxide.
mass of 75 moles of silicon dioxde:
4.5 kilograms of silicon dioxide is required to produce 3.00 kg of SiC.
Solid water is completely clear
Answer:
Living things in the ocean are able to move carbon from the atmosphere into surface waters.
Explanation:
The outer electrons of an element are called the valence electrons. They help make an element stable.
Cesium : 1 valence electron<span>.
Magnesium : 2 valence electrons</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).
