A mixture of compounds containing diethylamine, phenol, ammonia, and acetic acid is separated using liquid-liquid extraction as follows: Step 1: Concentrated HCl is added followed by draining the aqueous layer. Step 2: Dilute NaOH is added to the organic layer followed by draining the aqueous layer. Step 3: Concentrated NaOH is added to the organic layer followed by draining the aqueous layer. Which compound would you expect to be extracted into the aqueous layer after the addition of dilute HCl, step 1? Group of answer choices

Complete Question

The complete question is shown on the first uploaded image

The correct option is  ammonia

Explanation:

The mixture contains two base compound which are

           ammonia,

and     diethylamine

Now the addition of HCl which is  a strong acid in step 1  will cause the protonation of  the  two base compound , which makes the soluble hence resulting in them being extracted to the aqueous layer as represented in below

       

and

     

       

For cyclohexane compounds drawn in a chair conformation:   -axial bonds are vertical  -equatorial bonds are parallel to two bonds within the ring.  thus, as i assume the chair conformation is drawn:   -the x group is in an axial position, as are the five other vertical bonds.  -three axial bonds are on the top face of the ring  -the other three axial bonds are on the bottom face  the position of the second substituent on each ring carbon is equatorial.  gauche groups must be on an adjacent carbon such as carbon 6 and carbon 2, and also gauche groups are rotated by 60 degrees relative to each other.  drawing the newman projections for c1–c2 and c1–c6 aids in visualizing the groups that are gauche to the y group on c1.  click this link and watch some academic videos that may you more understand the topic 

If it releases 5 tons a day and there are 7 days a take that answer and multiply by 5 percent (0.05) to find the amount released in one week. leave a comment if you need more .