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prohojiy [21]
2 years ago
9

What is defined as the plants and animals and the physical surroundings, including the sun, air, soil, and water?

Chemistry
1 answer:
Sonja [21]2 years ago
8 0

Answer:

ecosystem

Explanation:

because population isnt it neither community or orgamism

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Which sample has more atoms in it? 150.0 g of gold or 10.0 g of lithium.
Deffense [45]

Answer:150g of gold

Explanation: There is a lot more gold and gold is significantly significantly more dense than lithium

6 0
3 years ago
A person has a mass of 63.4kg. What is the weight in pounds?
Evgen [1.6K]
If a person weighs 63.4 KG they will weigh 139.773 but if you estimate it which in most cases you do it would be 139.8 :)
3 0
1 year ago
Circle the atom with the largest atomic radius in each group
Dominik [7]

Answer:

The atomic radius increases down the group because more shell are added

Explanation:

Al >B

Na>Al

S>O

O>F

Br>Cl

Mg>Ca

4 0
3 years ago
A gas mixture containing oxygen, nitrogen, and carbon dioxide has a total pressure of 32.5 kPa. If Po2 =
HACTEHA [7]

Answer:

A gas mixture containing oxygen, nitrogen, and carbon dioxide has a total pressure of 32.5 kPa.

<u>The pressure for oxygen is 3 kPa</u>

Explanation:

According to Dalton's Law of Partial Pressure total exerted by the mixture of non-reacting gases is equal to sum of the partial pressure of each gas.

P_{total}=P_{1}+P_{2}+P_{3}

So,

For , a gas mixture containing oxygen, nitrogen, and carbon dioxide has a total pressure:

P_{total}=P_{O_{2}}+P_{N_{2}}+P_{CO_{2}}

P_{total} = 32.5kPa

P_{O_{2}} = 6.5kPa

P_{N_{2}} = 23.0kPa

Insert the values in :

P_{total}=P_{O_{2}}+P_{N_{2}}+P_{CO_{2}}

32.5 kPa = 6.5 kPa + 23.0 kPa +P_{CO_{2}}

32.5 kPa = 29.5 kPa +P_{CO_{2}}

P_{CO_{2}}= 32.5 - 29.5

P_{CO_{2}}= 3kPa

6 0
3 years ago
A ____________ alkene is more stable than a ____________ alkene because they have fewer steric interactions. In an elimination r
Vesna [10]

Answer:

See explanation

Explanation:

A <u>trans</u> alkene is more stable than a <u>cis alkene</u> because they have fewer steric interactions.

<em>⇒ In a cis alkene there is steric hindrance, because the methyl groups are on the same side of the double bond. </em>

<em>Because of this steric crowding, there are van der Waals repulsive forces between the electron clouds of the groups. </em>

<em> </em>

<em>This decreases the stability of the cis alkene.</em>

<em />

In an elimination reaction, a geometry where the β hydrogen and the leaving group are on opposite sides of the molecule is called <u>anti</u> periplanar.

<em> ⇒ 'Anti’ refers to the two functional groups lying on opposite sides of the plane of the bond</em>

In an <u>SN1 </u>mechanism, a nucleophile attacks the carbocation, forming a substitution product,

<em> ⇒ The SN1 reaction is a substitution reaction, and means "nucleophilic substitution".The "1" says that the rate-determining step is unimolecular. Thus, the rate equation is often shown as having first-order dependence on electrophile and zero-order dependence on nucleophile.</em>

while in an <u>E1</u><u> </u>mechanism, a base removes a β hydrogen from the carbocation, forming a new π-bond.

<em> ⇒ E1 indicates a elimination, unimolecular reaction</em>

<em>This implies that the rate determining step of the mechanism depends on the decomposition of a single molecular species.</em>

<em>.This is a classic elimination reaction – forming a new C–C(π) bond, and breaking a C–H and C–leaving group bond.</em>

CH3CH2Br and NaOH react by an <u>SN2</u><u> </u>mechanism.

<em> ⇒  It's a type of reaction mechanism that is common in organic chemistry, where one bond is broken and one bond is formed, synchronously, (in one step.) </em>

Stronger bases, like hydroxide, favor<u> E2</u> reactions, whereas weaker bases, like water favor, <u>E1</u> reactions

Disubstituted alkenes always have the possibility to exist as two different <u>Diastereomer.</u>

<em>Diastereomer are stereoisomers that are not mirror images of one another and are non-superimposable on one another. They exist (always) in 2 forms.</em>

<u>Elimination reactions</u> are regioselective, favoring formation of the more substituted and more stable alkene.

6 0
3 years ago
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