Answer:
1.2* 10³ rNe.
Explanation:
Given speed of neon=350 m/s
Un-certainity in speed= (0.01/100) *350 =0.035 m/s
As per heisenberg uncertainity principle
Δx*mΔv ≥\frac{h}{4\pi }
4π
h
..................(1)
mass of neon atom =\frac{20*10^{-3} }{6.22*10^{-23} } =3.35*10^{-26} kg
6.22∗10
−23
20∗10
−3
=3.35∗10
−26
kg
substituating the values in eq. (1)
Δx =4.49*10^{-8}10
−8
m
In terms of rNe i.e 38 pm= 38*10^{-12}10
−12
Δx=\frac{4.49*10^{-8} }{38*10^{-12} }
38∗10
−12
4.49∗10
−8
=0.118*10^{4}10
4
* (rNe)
=1.18*10³ rN
= 1.2* 10³ rNe.
Explanation:
This is the answer
Answer:
It would produce ethane (CH₃CH₃)
Explanation:
Ethylmagnesium bromide (CH₃CH₂MgBr) is a Grignard's reagent.
It is a highly reactive substance, and as any alkylmagnesium bromide
(R-CH₂MgBr) it reacts with water to produce an alkane (R-CH₃). R stands for any carbon structure bonded to that functional group.
<u>Answer:</u> The temperature of the system will be 1622 K
<u>Explanation:</u>
The equation relating the pre-exponential factor and activation energy follows:
where,
D = diffusion coefficient = 
= pre-exponential constant = 
= activation energy of iron in cobalt = 273,300 J/mol
R = Gas constant = 8.314 J/mol.K
T = temperature = ?
Putting values in above equation, we get:
Hence, the temperature of the system will be 1622 K
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).
