Answer: Option (d) is the correct answer.
Explanation:
It is given that molecular formula is
. Now, we will calculate the degree of unsaturation as follows.
Degree of unsaturation = 
= 
= 9 - 8 + 1
= 2
As the degree of unsaturation comes out to be 2. It means that this compound will contain one ring and one double bond.
Yes, this compound could be an alkyne as for alkyne D.B.E = 2.
But this compound cannot be a cycloalkane because for a cycloalkane D.B.E = 1 which is due to the ring only.
Thus, we can conclude that it is a cycloalkane is not a structural possibility for this hydrocarbon.
The atomic number of an element gives the proton and electron in the atom while the mass number gives the total number of protons and neutron
Its a base
as Na+ dissociates in the water and it has no basic nor acidic properties its neutral]
but the F- that also dissociates has certain basic properties
hope that helps
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).
1) Balanced equation
C3H8 + 5O2 -> 3 CO2 + 4 H2O
2) 0.700 L C3H8
Given the pressure and temperature do not change, the molar ratio is equivalent to volume ratio
1molC3H8 / 5 mol O2 => 1 L C3H8 / 5 L O2
0.700 L C3H8 / x L O2 = 1 L C3H8 / 5 L O2 => x = 0.700 L C3H8 * 5 L O2 / 1 L C3H8
x = 3.500 L O2
3) CO2 produced
1 L C3H8 / 3 L CO2 = 0.700 L C3H8 / x L CO2 =>
x = 0.700 L C3H8 * 3 L CO2 / 1 L C3H8 = 2.100 L CO2
4) Water vapor produced
1) 1 L C3H8 / 4 L H2O = 0.700 LC3H8 / x L H2O =>
x = 0.700 L C3H8 * 4 L H20 / 1 L C3H8 = 2.800 L H2O