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Vsevolod [243]
4 years ago
14

Which power source uses the earth’s internal heat?

Chemistry
1 answer:
Nataly_w [17]4 years ago
5 0

Answer:

Its geothermal energy.

Explanation:

hope this helps

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Which of the following lists the characteristics that all matter has?
motikmotik
It has mass and takes up space is correct. 
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3 years ago
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What do geologists call the underground molten mixture of rock-forming substances, gases, and water that is found in the mantle?
Likurg_2 [28]

Answer:

B.) Magma

Explanation:

Lava - Magma that reaches Earth's through a volcanic vent

Magma - Composed of molten mixture of rock-forming substances, gases and water

Batholith - Very large igneous intrusion extending deep in the earth's crust

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One set of environmental factors lists ONLY biotic factors. That is
Dmitry_Shevchenko [17]
I hope this helps you

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3 years ago
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What number of particles will BaBr2 make in solution?<br><br> 1<br> 2<br> 3<br> or 4?
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One Ba2+ and two Br- ions will be there.

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3 0
3 years ago
What is the main side reaction that competes with elimination when a primary alkyl halide is treated with alcoholic potassium hy
Elanso [62]

Answer:

The main competing reaction when a primary alkyl halide is treated with alcoholic potassium hydroxide is SN2 substitution.

Explanation:

The relative percentage of products of the reaction between an alkyl halide and alcoholic potassium hydroxide generally depends on the structure of the primary alkylhalide. The attacking nucleophile/base in this reaction is the alkoxide ion. Substitution by SN2 mechanism is a major competing reaction in the elimination reaction intended.

A more branched alkyl halide will yield an alkene product due to steric hindrance, similarly, a good nucleophile such as the alkoxide ion may favour SN2 substitution over the intended elimination (E2) reaction.

Both SN2 and E2 are concerted reaction mechanisms. They do not depend on the formation of a carbocation intermediate. Primary alkyl halides generally experience less steric hindrance in the transition state and do not form stable carbocations hence they cannot undergo E1 or SN1 reactions.

SN2 substitution cannot occur in a tertiary alkyl halides because the stability of tertiary carbocations favours the formation of a carbocation intermediate. The formation of this carbocation intermediate will lead to an SN1 or E1 mechanism. SN2 reactions is never observed for a tertiary alkyl halide due to steric crowding of the transition state. Also, with strong bases such as the alkoxide ion, elimination becomes the main reaction of tertiary alkyl halides.

7 0
3 years ago
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