An optically active alkyne A (C10H14) can be catalytically hydrogenated to butylcyclohexane. Treatment of A with C2H5MgBr liberates no gas. Catalytic hydrogenation of A over Pd/C in the presence of quinoline poison and treatment of the product B with O3 and then H2O2 gives an optically active tricarboxylic acid C8H12O6. (A tricarboxylic acid is a compound with three –CO2H groups.) Give the structure of A (without stereochemistry).

How are ionic bonds formed and what is the attractive force within an ionic bond

For a research project, a student decided to test the effect of the lead(ii) ion (pb2+) on the ability of salmon eggs to hatch. this ion was obtainable from the water‐soluble salt, lead(ii) nitrate, which the student decided to make by the following reaction. pbo(s) + 2 hno3(aq) → pb(no3)2(aq) + h2o losses of product for various reasons were expected, and a yield of 86.0% was expected. in order to have 5.00 g of product at this yield, how many grams of pbo should be reacted? (assume that sufficient nitric acid, hno3, would be used.)

One student said that the investigation was not valid (a fair test). write a plan for the investigation that includes improvements to the method and apparatus