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Dahasolnce [82]
3 years ago
7

Which is an example of a heterogeneous catalyst?

Chemistry
2 answers:
N76 [4]3 years ago
8 0
An example of a heterogeneous catalyst is a catalytic converter. A catalytic converter is an emissions control device that converts toxic pollutants in exhaust gas to less toxic pollutants by catalyzing a redox reaction (oxydation or reduction). 
g100num [7]3 years ago
5 0

Answer:

catalytic converter

Explanation:

A heterogeneous catalyst is one that has a phase different from the reactant molecules. A catalyst speeds up a chemical reaction by lowering the activation energy required to start the reaction. But a catalyst does not undergo any change in the chemical process. Catalysts in a catalytic converter are metallic palladium or platinum that react with the hydrocarbons and carbon monoxide from the exhausts of a car to form carbon dioxide and water.

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Discuss how industrial chemistry would be of relevance to the government
icang [17]

Why is industrial chemistry important?

Industrial chemistry plays an important role in our society. Thousands of products and applications have increased the standard of living of billions of people in the last century. Life today without the benefits of industrial chemistry and the chemical industry would be difficult and of low quality

8 0
3 years ago
Students in Ms. Brown’s class are on a field trip at the aquarium. They observe the following biotic and abiotic factors in the
Virty [35]

Rocks - abiotic

Coral - biotic

Seaweed - biotic

Clownfish- biotic

sea turtle - biotic

water system - abiotic

7 0
3 years ago
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How many atoms are there in 5.8 mol of iron
kkurt [141]
4.0 mol. 6.02 x 10. 23 atoms. 3. How many moles are in 2.5g of lithium? 2.5 grams Li. 1 mole. = 0.36 mol. 6.9 g. 4. Find the mass of 4.8moles of iron. 4.8 moles.
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3 years ago
3) Explain why the standard enthalpy of vaporization, (Delta)Hvap, values for each set of compounds below are not the same.
Amanda [17]

Answer:

a. CH4 is only held together by London dispersion forces since any dipoles cancel out due to symmetry. On the other hand H2O  has strong hydrogen bonds

b. PH3 has dipole-dipole forces while NH3 is held together by stronger hydrogen bonding

c. C2H6 and C3H8 . Both substances are held together by London dispersion forces since any dipoles cancel out due to symmetry. However C3H8 has the stronger London dispersion forces of the two because it is a larger molecule,

d. BH3 is held together by London dispersion forces since any dipoles cancel out due to symmetry while OF2​ is held together by stronger dipole-dipole forces

7 0
3 years ago
I honestly am stuck with this question for at least 30 minutes. I NEED AN EXPERT AND HELP FAST! PLEASE HELP ME!!! ​
vovikov84 [41]

Answer:

Here's what I get  

Explanation:

1. Synthesis

(a) Preparation of Grignard reagent

React allyl bromide with magnesium in dry ether.

(b) Grignard reaction

Add allylmagnesium bromide to methyl phenyl ketone. Convert the alkoxide to the alcohol by treatment with aqueous ammonium chloride.

(c) 1,2-Dihydroxylation

React the alkene with tert-butyl peroxide and a catalytic amount of hydrogen peroxide. Decompose the osmate ester with aqueous sodium hydroxide.

2. Mechanism

Here are my proposed steps for the mechanisms.

(a) The 65 % Product

(i) Protonation of the secondary alcohol

(ii) Loss of the protonated OH group to form a secondary carbocation

(iii) Alkyl migration/ring expansion to form a more stable tertiary carbocation

(iv) Deprotonation to form the ketone

(b) The 25 % product

(a) Protonation of the tertiary alcohol

(ii) Loss of the protonated OH group to form a tertiary carbocation

(iii) Hydride shift to form a protonated carbonyl group

(iv) Deprotonation to form the ketone

(c) The 10 % product

(i) Electrophilic aromatic attack by the cation formed in step (b)(ii) to form a cyclopropane intermediate.

(ii) Cleavage of a cyclopropane bond to regenerate the aromatic ring and form a protonated carbonyl group

(iii) Deprotonation to form an aldehyde.

5 0
3 years ago
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