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ivolga24 [154]
2 years ago
14

Explain preparation of alkanes C--C from industrial source for industrial preparation of alkane​

Chemistry
1 answer:
Dmitrij [34]2 years ago
4 0
Alkanes can be prepared from carboxylic acid via the removal of carbon dioxide. This process is known as decarboxylation. It produces alkane with a carbon atom lesser than that present in the carboxylic acid.
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What is the mass of carbon monoxide (CO) gas if the gas occupies a volume of 4.1 L at 2.0 atm of pressure and -73oC?
Stels [109]

Answer:

1.7

Explanation:

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2 years ago
Which best describes teratogen
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A teratogen is an exposure (substance, organism or process) in pregnancy that has a harmful effect on the fetus. Teratogens can be diseases, medications, drugs and environmental exposures.
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How much °f of 35°C ? <br>help me please<br>​
MakcuM [25]

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Explanation:

6 0
3 years ago
There are 50 fish in the pond that have tags. You catch 25 fish, and 5 of them have tags. What is the best estimate of the numbe
sergeinik [125]

Answer: 250


Explanation:


You work this problem by using proportions.


A proportion is the equalization of two ratios.


Here you assume that the ratio of fish with tags to total fish that you catch is the same than the ratio of fish with tags to total fish in the pond.


Mathematically:

  • 5 fish with tag / 25 fish = 50 fish with tag / x
  • 5 / 25 = 50 / x

Solve for x:

  • Multiplication property of equality: x × 5 = 50 × 25
  • Division property of equality: x = 50 × 25 / 5
  • Result: 250
8 0
2 years ago
Read 2 more answers
List and explain the four most important factors that control the relative reactivity of a carbonyl-containing functional group
ioda

Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.

Discussion:

1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.

2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.

3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.

4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.

Learn more about carbonyl here:

brainly.com/question/21440134

#SPJ4

8 0
1 year ago
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