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frez [133]
2 years ago
8

Select all of the answers that apply.

Chemistry
2 answers:
Softa [21]2 years ago
7 0

Answer:

winds :)

Explanation:

katovenus [111]2 years ago
6 0

\mathfrak{\huge{\orange{\underline{\underline{AnSwEr:-}}}}}

Actually Welcome to the Concept of the Geography.

Surface currents in a ocean or a sea are driven by Winds.

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For an experiment, you place 15 g of ice with a temperature of -10 C into a cup and label
melamori03 [73]
The correct answer is c. Temperature is the average kinetic energy of a sample so if two samples have the same temperature they will also have the same average kinetic energy. I hope this helps. Let me know if anything is unclear.
6 0
2 years ago
Read 2 more answers
The following reactions take place in the ozone layer by the absorption of ultraviolet light.
____ [38]

Answer:

Option B will require a shorter wave length of light.

Explanation:

The bonding between Ozone (O3) and Oxygen (O2) can be used to explain why the breaking of oxygen into Oxygen radicals will require a shorter wave length.

  • The bond between Oxygen (O2) is a double bond while Ozone (O3) has an intermediate bond between a double bond and a single bond.
  • The bond order of Oxygen (O2) is equals 2 while that of Ozone (O3) is 1.5. Since the bond order of oxygen is higher, it will require more energy to break the bond compared to breaking the Ozone (O3) bond.
  • Recall that Energy is inversely proportional to wave length.
  • So it will require a shorter wave length to break the Oxygen (O2) into its radicals.
5 0
3 years ago
Is boron an element a compound a heterogeneous mixture or a homogeneous mixture?
liberstina [14]
The answer is heterogeneous mixture<span> because the </span>blood<span> cells are physically separate from the </span>blood<span> plasma.</span>
3 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
3 years ago
In a two-step synthesis, C6H11Br is converted into C6H12O. From the structure of the product, molecular formula of the starting
tamaranim1 [39]

Answer:

See explanation below

Explanation:

The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.

Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.

First, all what we have here is an acid  base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.

In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.

See picture 2, for mechanism

8 0
3 years ago
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