Each of the organic compounds mentioned has a general formula so that we can identify the classification of a certain substance. The compound CH₃CH₂OH is an alcohol because it follows the general formula R-OH, where R is a hydrocarbon chain. In this case, the hydrocarbon chain is ethane. When a hydroxyl functional group is attached, it becomes an alcohol whose name is ethanol.
Explanation:
substance Q could be <em><u>oxygen (O2)</u></em>
substance R could be <em><u>carbon</u></em><em><u> </u></em><em><u>d</u></em><em><u>i</u></em><em><u>o</u></em><em><u>x</u></em><em><u>i</u></em><em><u>d</u></em><em><u>e</u></em><em><u> </u></em><em><u>(</u></em><em><u>C</u></em><em><u>O</u></em><em><u>2</u></em><em><u>)</u></em>
Answer:
Less
Explanation:
Since [Cu(NH3)4]2+ and [Cu(H2O)6]2+ are Octahedral Complexes the transitions between d-levels explain the majority of the absorbances seen in those chemical compounds. The difference in energy between d-levels is known as ΔOh (ligand-field splitting parameter) and it depends on several factors:
- The nature of the ligand: A spectrochemical series is a list of ligands ordered on ligand strength. With a higher strength the ΔOh will be higher and thus it requires a higher energy light to make the transition.
- The oxidation state of the metal: Higher oxidation states will strength the ΔOh because of the higher electrostatic attraction between the metal and the ligand
A partial spectrochemical series listing of ligands from small Δ to large Δ:
I− < Br− < S2− < Cl− < N3− < F−< NCO− < OH− < C2O42− < H2O < CH3CN < NH3 < NO2− < PPh3 < CN− < CO
Then NH3 makes the ΔOh higher and it requires a higher energy light to make the transition, which means a shorter wavelength.
Ok we can use boyle’s law (stating that P is proportional to V) to make the equation (P1V1) =(P2V2).
once we’ve done this, we can plug in the numbers:
(800•500) = (200•V2)
and then we get that
V2= 2000 ml
hope this helps!! :)
Igneous <span>rock ! Of course oh how i miss middle school.........</span>