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siniylev [52]
2 years ago
15

4) The initial rate of the reaction between substances P and Q was measured in a series of

Chemistry
1 answer:
ASHA 777 [7]2 years ago
6 0

Answer:

The initial rate of the reaction between substances P and Q was measured in a series of

experiments and the following rate equation was deduced.

rate = k[P]^{2} [Q]

Complete the table of data below for the reaction between P and Q

Explanation:

Given rate of the reaction is:

rate= k[P]^{2} [Q]\\=>[Q]=\frac{rate}{k.[P]^{2} } \\and \\\\\\\ [P]=\sqrt{\frac{rate}{k.[Q]} }

Substitute the given values in this formulae to get the [P], [Q] and rate values.

From the first row,

the value of k can be calulated:

k=\frac{rate}{[P]^{2}[Q] } \\  =\frac{4.8*10^-3}{(0.2)^{2} 2. (0.30)} \\ =0.4

Second row:

2. Rate value:

rate =0.4* (0.10)^{2} * (0.10)\\\\        =4.0*10^-3mol.dm^-3.s^-1

3.Third row:

[Q]=\frac{rate}{k.[P]^{2} } \\     =9.6*10^-3 / (0.4 *(0.40)^{2} \\    =0.15mol.dm^{-3}

4. Fourth row:

[P]=\sqrt{\frac{rate}{k.[Q]} }\\=>[P]=\sqrt{\frac{19.2*10^-3}{0.60*0.4} } \\=>[P]=0.283mol.dm^{-3}

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A certain hydrocarbon has a molecular formula of C9H16. Which of the following is not a structural possibility for this hydrocar
snow_tiger [21]

Answer: Option (d) is the correct answer.

Explanation:

It is given that molecular formula is C_{9}H_{16}. Now, we will calculate the degree of unsaturation as follows.

Degree of unsaturation = C_{n} - \frac{\text{monovalent}}{2} + \frac{\text{trivalent}}{2} + 1

                                  = 9 - \frac{16}{2} + 1

                                  = 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.

6 0
3 years ago
The atomic number of an element gives the number of __ and __in the atom while the mass number gives the total number of__and__
posledela
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
8 0
3 years ago
Is naf an acidic, basic, or neutral solution?
lara31 [8.8K]
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 
4 0
3 years ago
Determine whether each description applies to electrophilic aromatic substitution or nucleophilic aromatic substitution.
Alborosie

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).

3 0
3 years ago
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1) Balanced equation

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x = 3.500 L O2

3) CO2 produced

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x = 0.700 L C3H8 * 3 L CO2 / 1 L C3H8 = 2.100 L CO2

4) Water vapor produced

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x = 0.700 L C3H8 * 4 L H20 / 1 L C3H8 = 2.800 L H2O
3 0
3 years ago
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