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Darina [25.2K]
3 years ago
11

Dalton's atomic theory stated?

Chemistry
1 answer:
kondaur [170]3 years ago
3 0
John Dalton in d year 1808 proposed d atomic theory.. 1.All elements are made up of small, indivisble particles called atoms. 2.Atoms can neither be created nor destroyed. 3.Atoms of d same element are alike in every aspect, &differ from atoms of all other elements. 4. When atoms combine with other atoms, they do so in simple ratios.
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What is shown by the structural formula of a molecule or polyatomic ion?
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Answer : Option A) the arrangement of bonded atoms.


Explanation : A structural formula of certain molecule depicts the way the atoms are arranged in that particular molecule in any polyatomic species. It helps in deciding the chemical properties of that polyatomic molecule.
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6th grade science i will give brainliest
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0.2 m/s! keep in mind, speed= distance divided by time :D
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A chemist titrates 130.0mL of a 0.4248 M lidocaine (C14H21NONH) solution with 0.4429 M HBr solution at 25 degree C . Calculate t
jeka57 [31]

Answer:

pH = 3.36

Explanation:

Lidocaine is a weak base to be titrated with the strong acid HBr, therefore at equivalence point we wil have the protonated lidocaine weak conjugate acid of lidocaine which will drive the pH.

Thus to solve the question we will need to calculate the concentration of this weak acid at equivalence point.

Molarity = mol /V ∴ mol = V x M

mol lidocaine = (130 mL/1000 mL/L) x 0.4248 mol/L = 0.0552 mol

The volume of 0.4429 M HBr required to neutralize this 0.0552 mol is

0.0552 mol x  (1L / 0.4429mol) = 0.125 L

Total volume at equivalence is  initial volume lidocaine + volume HBr added

0 .130 L +0.125 L = 0.255L

and the concentration of protonated lidocaine at the end of the titration will be

0.0552 mol / 0.255 L = 0.22M

Now to calculate the pH we setup our customary ICE table for  weak acids for the equilibria:

protonated lidocaine + H₂O   ⇆  lidocaine + H₃O⁺

                      protonated lidocaine          lidocaine        H₃O⁺

Initial(M)               0.22                                       0                  0

Change                   -x                                      +x                 +x

Equilibrium          0.22 - x                                  x                    x

We know for this equilibrium

Ka = [Lidocaine] [H₃O⁺] / [protonaded Lidocaine] =  x² / ( 0.22 - x )

The Ka can be calculated from the given pKb for lidocaine

Kb = antilog( - 7.94 ) = 1.15 x 10⁻⁸

Ka = Kw / Kb = 10⁻¹⁴ / 1.15 x 10⁻⁸  = 8.71 x 10⁻⁷

Since Ka is very small we can make the approximation 0.22  - x  ≈ 0.22

and solve for x. The pH  will then  be the negative log of this value.

8.71 x 10⁻⁷  = x² / 0.22 ⇒ x = √(/ 8.71 X 10⁻⁷ x 0.22) = 4.38 x 10⁻⁴

( Indeed our approximation checks since 4.38 x 10⁻⁴ is just 0.2 % of 0.22 )

pH = - log ( 4.4x 10⁻⁴) = 3.36

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3 years ago
Activation energy is ____. (1 point)
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See attached figure for the structure.

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2) phenolic hydroxide group: R-OH, were the hydroxyl group is bounded to a carbon from the benzene ring

3) ether group: R-O-R, were hydrogen is bounded through sigma bonds to carbons

Now for the hybridization we have:

The carbon atoms involved in the benzene ring and the red carbon atom (from the aldehyde group) have a <u>sp²</u> hybridization because they are involved in double bonds.

The carbon atom from the methoxy group (R-O-CH₃) and the blue oxygen's have a  <u>sp³</u>  hybridization because they are involved only in single bonds.

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