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Pavlova-9 [17]
3 years ago
14

Help pls pls pls I really need this answer

Chemistry
1 answer:
blagie [28]3 years ago
5 0

Answer:

I never did this but i think its d 37.5٪ lmk if i got it right pls and srry if i didnt

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List three factors that affect the rate of a chemical reaction<br>​
Darina [25.2K]

Explanation:

Three factors that affect the rate of a chemical reaction

are listed below:

1.presence/absence of catalyst

2.temperature

3.nature of reactants

HOPE THIS WILL HELP U

6 0
3 years ago
Explain how to write formulas and oxidation numbers
PolarNik [594]
Oxidation number, also called oxidation state, the total number of electrons that an atom either gains or loses in order to form a chemical bond with another atom. Oxidation numbers also play an important role in the systematic nomenclature of chemical compounds. By definition, the oxidation number of an atom is the charge that atom would change.

When writing the formula for the ionic compound, the cation comes first, followed by the anion, both with numeric subscripts to indicate the number of atoms of each. Polyatomic ions are a set of covalently bonded atoms that have an overall charge, making them an ion.

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3 0
2 years ago
What is the correct term for plants releasing water from their leaves which then evaporates?
ratelena [41]

Answer:

Transpiration is the correct answer mark me brainliest

7 0
3 years ago
The Fischer esterification mechanism is examined in this question. The overall reaction is: Benzoic acid, C H 3 O H and H C l re
elena55 [62]

Answer:

See explanation and image attached

Explanation:

Fischer esterification is a type of reaction used  to convert carboxylic acids to ester in the presence of excess alcohol and a strong acid which acts as a catalyst. Another final product formed in the reaction is water.

The mechanism for the fischer esterification of Benzoic acid and  C H 3 O H in the presence of HCl as the catalyst is shown in the image attached to this answer.

The final products of the reaction are methyl benzoate, water and H^+ as shown in the image attached.

4 0
3 years ago
G what is the difference between the sidechains of leucine and isoleucine? select one:
statuscvo [17]

c. Isoleucine has a carbon “branched” closer to the alpha carbon than does leucine.

The structure of leucine is CH3CH(<u>CH3</u>)CH2CH(NH2)COOH.

The structure of isoleucine is CH3CH2CH(<u>CH3</u>)CH(NH2)COOH.

In leucine, the CH3 group is <em>two carbons away</em> <em>from</em> the α carbon; in isoleucine, the CH3 group is on the carbon <em>next to</em> the α carbon.

Thus, <em>isoleucine</em> has the closer branched carbon.

“One is charged, the other is not” is i<em>ncorrect</em>. Both compounds are uncharged.

“One has more H-bond acceptors than the other” is <em>incorrect</em>. Each acid has two H-bond acceptors — the N in the amino and the O in the carbonyl group.

“They have different numbers of carbon atoms” is <em>incorrec</em>t. They each contain six carbon atoms.

4 0
4 years ago
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