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Brut [27]
3 years ago
11

Someone help. trying to past this test but keep failing on this question.

Chemistry
1 answer:
Katarina [22]3 years ago
8 0
A or b sorry if I’m wrong
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Chemical properties of acetic acid
alex41 [277]
I don't think that there is a chemical property of it. here are the physical properties:
Melting Point:
16.6°C 
Boiling Point:
117.9°C<span>
</span>
<span>Density (g/cm3):
</span>
1.0446 at 25°C 9

<span>1 atm pressure</span>
7 0
3 years ago
Can somebody help me with my Abiotic vs. Biotic Knowledge Check?
yawa3891 [41]

Answer:

abiotic and biotic check

Explanation:

Abiotic is something that is not living

Ex:air

Biotic is something that is living

EX :Plants

4 0
3 years ago
What happend if NH3+ HJ
Liula [17]
Are you sure you copied that down correctly? I know what NH3 is but HJ I am comming up blank on. The only thing HJ I know is hebdojoule which is unit system.
Are you doing chemical balancing?
6 0
3 years ago
Where within the cell does the process of respiration take place?
Licemer1 [7]

Answer:

cytoplasm

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4 0
2 years ago
Read 2 more answers
Write the structure of the product that would be formed from the S(
prisoha [69]

Answer:The product formed on reaction with hydroxide ion as nucleophile is 2R-hexane-2-ol.

The product formed on reaction with water would be a 50:50 mixture of

2S-hexane-2-ol. and 2R-hexane-2-ol.

Explanation:

2S-iodohexane on reactiong with hydroxide ion would undergo SN² substitution reaction that is substitution bimolecular. Hydroxide ion has a negative charge and hence it is a quite good  nucleophile .

The rate of a SN² reaction depends on both the substrate and nucleophile . Here the substrate is a secondary carbon center having Iodine as a leaving group.SN² reaction  takes place here as hydroxide ion is a good nucleophile and it can attack the secondary carbon center from the back side leading to the formation of 2R-hexane-2-ol.

In a SN² reaction since the the nucleophile attacks from the back-side so the product formation takes place with the inversion of configuration.

When the same substrate S-2-iodohexane undergoes a substitution reaction with water as a nucleophile then the reaction occurs through (SN¹) substitution nucleophilic unimolecular mechanism .

The rate of a SN¹ reaction depends only on the nature of substrate and is independent of the nature of nucleophile.

The SN¹ reaction is a 2 step reaction , in  the first step leaving group leaves leading to the formation of a carbocation and once the carbocation is formed then any weaker nucleophile or even solvent molecules can attack leading the formation of products.

In this case a secondary carbocation would be generated in the first step and then water will attack this carbocation to form the product in the second step.

The product formed on using water as a nucleophile would be a racemic mixture of R and S isomers of hexane -2-ol in 50:50 ratio. The two products formed would be 2R-hexane-2-ol and 2S-hexane-2-ol.

Kindly refer the attachment for reaction mechanism and structure of products.

8 0
3 years ago
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