Answer:
By far the most important use of alkenes is in the making of plastics as plastics are used in almost everything.
Explanation:
Alkenes themselves aren't used much in everyday life however Alkenes are very important to industrial synthesis as it is relatively easy to turn them into other things.
Alkenes can be turned into polymers or plastics through addition reactions and the most common ethene is turned into everything from plastic bags to bottles.
Alkenes can also be turned into alcohols. most commonly propene is used as a feedstock to produce butanol and other products useful in industry or for production
Explanation:
Can you be my friend in here
Answer:
Three primary reasons. First, there is simply more water-covered places than dry ground places for the animals and plants to have lived. Second, the seas are much more crowded with the kinds of life that leave fossils than the land is. Third, the process that form fossils work very well under water.
Explanation:
<h2>
NH3 is a weak alkali that does not dissociate fully into its solution. Which of the following is true about NH3?
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A. It has a very low pH.
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B. It's dissociation is a reversible reaction.
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C. It has a high H+ concentration.
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D. It will release all of its OH- ions.</h2>
Explanation:
<h3>
NH3 is a weak alkali that does not dissociate fully into its solution: It's dissociation is a reversible reaction.
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Reactions are also :
Reversible reaction
A reaction in which products can combine back to give reactants under same given condition .
Example : N₂+H₂-------NH₃
Irreversible reaction
A reaction in which the products cant combine back to give reactants under same set of conditions .
Example : Burning of paper
Answer:
Axial
Explanation:
In the most stable conformation of Cis-3-tert-Butylcyclohexanol, the tert-butyl group is at equatorial position and the alcohol group is in the axial position.
If the tert-butyl group is placed in equatorial position, repulsions are minimized. The bulkier the group, the greater the energy difference between the axial and equatorial conformers. Hence for a ring having a bulky substituent, such bulky substituent is better placed in the equatorial position.
The energy difference between the conformers of Cis-3-tert-Butylcyclohexanol is so high that the compound is almost "frozen" in a conformation where the tert-butyl groups are equatorial and the -OH groups are axial. This conformer is more stable by 24 KJ/mol.
