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jek_recluse [69]
3 years ago
5

What is the Iupac name for CH3CHIH3​

Chemistry
1 answer:
frozen [14]3 years ago
8 0

Answer:

Acetone | CH3COCH3 - PubChem

Explanation:

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Which of the following statements are correct? More than one answer may be correct.
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E, only one statement is correct

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Absorption is favoured by heating the solution containing the colored impurity.

Pleaseee! Mark me brainliest

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2 years ago
A hot cup of water has fewer molecules than a hot tub of water. This same cup of
Mrac [35]

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Paladinen [302]

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c

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What type of landforms do we have in Florida?
Bingel [31]

Answer:

Flora and Fauna

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Predict the two most likely mechanisms for the reaction of 1-iodohexane with potassium tert-butoxide.
Rudiy27

Answer:

C) SN2 and E2

Explanation:

For this question, we have analyzed the <u>substrate</u> and the <u>base/nucleophile</u>. The substrate, in this case, is 1-iodohexane and the base/nucleophile is potassium tert-butoxide.

<u>Substrate</u>

<u />

In the 1-iodohexane the iodide "I" is bonded to a primary carbon (carbon 1). Therefore we will have a <u>primary substrate</u>. If we have a primary substrate an Sn1 can not take place. We can not have a <u>primary carbocation</u> due to this instability. So, we can disccard options A) and B).

<u>Base/nucleophile</u>

<u />

In the potassium tert-butoxide we have an ionic compound. A positive charge is placed in the potassium atom a negative charge is placed in the oxygen of the ter-butoxide ion. So, we will have a <u>strong base</u> (a molecule with the ability to remove electrons) and a <u>strong nucleophile</u> (a molecule with ability to bond with an electrophile). With all this in mind, w<u>e can not have an E1 reaction</u>.

With both analyses, the answer is C).

See figure 1

I hope it helps!

6 0
3 years ago
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