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kirill115 [55]
3 years ago
6

Plz help with number 4

Chemistry
1 answer:
In-s [12.5K]3 years ago
6 0
Extensive: mass, length, volume
Inexpensive: color, density, aluminum
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Why is it important to control the reaction rate of the chemical process
xxTIMURxx [149]
Mg+2HCl=MgCl_2+H_{2(g)}

The reaction creates dihydrogen, hence if it's uncontrolled it could lead to potentially dangerous amounts of gas being released at once.
8 0
3 years ago
4. A student was not sure that she accurately recorded the final temperature of her melting point sample. Therefore, she decided
Mumz [18]

Answer:

AWF DSF

Explanation:

W AFSDDDDDDDDD

3 0
2 years ago
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
Compound A melts at 801o C and is soluble
Karo-lina-s [1.5K]

Explanation:

Organic compounds are defined as the compounds which contain carbon as their main element. For example, CH_{3}OH is an organic compound.

Generally, organic compounds are non-polar in nature and due to the presence of covalent bonding organic compounds have low melting point.

As compound A melts at 801^{o}C and is soluble  in water. This means it is an ionic compound as it has high melting point and it is also polar in nature.

Whereas compound B melts at 24^{o}C and is insoluble  in water. This means that this compound has covalent bonding and it is also non-polar in nature . Hence, it is more likely to be organic in nature.

Thus, we can conclude that compound B is more likely to be an organic

compound.

7 0
3 years ago
HELP!!! I WILL RATE BRAINLIEST!!!
ad-work [718]

Answer:

it D yo

Explanation:

7 0
3 years ago
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