For the acids, use the formula pH = -log[H+). (Because HCI has 1 H+ ion per formula unit, [H] equals the

molarity.) For water, use what you know about the pH of neutral solutions. For the bases, examine and

extend the pattern. DONE

0.1 M

0.001 M

HCI

HCI

0.00001 M

HCI

Distilled

Water

0.00001 M

0.001 M

NaOH

NaOH

0.1 M

NaOH



000000000

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 

High-energy and unstable.

Sorry i dont understand the question can you rephase it?