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stiv31 [10]
2 years ago
10

The use of nuclear power in place of coal, oil, and natural gas greatly reduces emissions of carbon dioxide and other greenhouse

gases. TRUE FALSE
Chemistry
2 answers:
xz_007 [3.2K]2 years ago
8 0
False!  It makes emissions greater
vekshin12 years ago
6 0
I think the answer is False
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What is the electron structure of a sodium atom?
nordsb [41]

Answer:

1s22s22p63s1 is the electronic configuration of sodium.

Explanation:

7 0
3 years ago
Read 2 more answers
An undergraduate weighed out 20grams of sodium hydroxide pellets. If Na =23, O = 16 andH = 1, What is the mole of this sodium hy
tatuchka [14]
The answer would be .5 mols because you take the total amount of grams, which is 20, and you had up the molar mass of sodium hydroxide, which would be 40. After you have this you would set this up as a stochiometry equation. With 1 mol on top you dived 20/40 to cancel out your grams. This leaves you with .5 mols

3 0
3 years ago
What makes an acid a strong acid in water makes a base or weak base
11Alexandr11 [23.1K]
It’s ph level on the ph scale. 1-3 is a strong acid, 4-6 is a weak acid, 7 is neutral, 8-10 is a weak base, and 10-14 is a strong base.
8 0
2 years ago
What is included in a compaarative investigation
Minchanka [31]

a scientific question

6 0
3 years ago
Sodium tert-butoxide (NaOC(CH3)3) is classified as bulky and acts as Bronsted Lowry base in the reaction. It is reacted with 2-c
IceJOKER [234]

Answer:but-1-ene

Explanation:This is an E2 elimination reaction .

Kindly refer the attachment for complete reaction and products.

Sodium tert-butoxide is a bulky base and hence cannot approach the substrate 2-chlorobutane from the more substituted end and hence major product formed here would not be following zaitsev rule of elimination reaction.

Sodium tert-butoxide would approach from the less hindered side that is through the primary centre and hence would lead to the formation of 1-butene .The major product formed in this reaction would be 1-butene .

As the mechanism of the reaction is E-2 so it will be a concerted mechanism and as sodium tert-butoxide will start abstracting the primary hydrogen through the less hindered side simultaneously chlorine will start leaving. As the steric repulsion in this case is less hence the transition state is relatively stabilised and leads to the formation of a kinetic product 1-butene.

Kinetic product are formed when reactions are dependent upon rate and not on thermodynamical stability.

2-butene is more thermodynamically6 stable as compared to 1-butene  

The major product formed does not follow the zaitsev rule of forming a more substituted alkene as sodium tert-butoxide cannot approach to abstract the secondary proton due to steric hindrance.

5 0
3 years ago
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