If the experiment were repeated using a cuvettes with a path length of 2.0 cm, how would that affect the absorbance values for the Co2 solutions (if at all), assuming all of the concentrations remained unchanged?

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 

A1 a 2 a 3 ooh lol i think that's it

3is your answer to yuor question

2poclâ‚(g) ⇜ 2 pclâ‚(g) + oâ‚‚(g) â†gâ° = (2 mol)î”gfâ°(pclâ‚) – (2 mol)î”gfâ°(poclâ‚) = (2 mol)(–270 –(–502) kj/mol) â†gâ° = + 464 kj = â†hⰠ– tî”sâ° î”sâ° = 179 j/k ⇒ â†hâ° = â†gâ° + (298 k)(179 j/k) = –411 kj assuming that î”hâ° and î”sâ° do not depend on temperature, the temperature at which â†gâ° = 0 is where t = â†hâ°/î”sâ° = (–411 kj)/(0.179 j/k) = 2294 k. at that temp. keq = 1 for the reaction.