Answer the following questions using the given information. Solution A-408.0 g of H2SO4 (sulfuric acid) was poured into a 1000 ml beaker and then water was added until the volume reached 800 mL
Solution B - 25.5 g of H2SO4 was poured into a 100 ml beaker and then water was added until the volume reached 25 ml
Level 2 - A 12 g strip of magnesium is then added to each beaker (both are at room temperature), which solution should react faster with the
magnesium, justify using the concentration of both solutions? At the molecular level, why do you think that solution will react faster?
Level 3 - Using the information and reactants from the level 2 question, how would you design a test to verify this? What data would you be
collecting to support your claim from the level 2 problem?

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 

Outermost (valence) electrons