This pair of molecules are . Two ball-and-stick models of molecules. The first molecule consists of five black balls, which form a cyclical structure. Each black ball has two white balls attached. The second molecule has a chain of five black balls connected successively. Each of the two black balls, which are at the ends of the chain, has three white balls attached. Each of the three other black balls has two white balls attached. identical not isomers enantiomers structural isomers cis-trans isomers (geometric isomers)

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 

They can measure  the amount of energy gained or lost

Hbr dissociates to form h+ and br-ca(oh)2 dissociates to form ca2+ and 2oh-the h+ and oh- react to form waterassuming the reactants are dissolved in water, the net reaction is h+ + oh- —> h2oif you’re asked to show all components of the reaction, the complete reaction is 2hbr + ca(oh)2 —> cabr2 + 2h2o