2C6H14 + 13O2 ---> 6CO2 +14H2O
M(C6H14)=12.011*6 +1.008*14 ≈ 86.17 g/mol
86.17 g C6H14 is 1 mole.
2C6H14 + 13O2 ---> 6CO2 +14H2O
from reaction 2 mol 6 mol
from the problem 1 mol 3 mol
M(CO2)= 12.011 + 2*15.999= 44.009 g/mol
3 mol CO2*44.009 g/1 mol CO2 ≈ 132.0 g CO2
Answer : 132.0 g CO2
Hello!
To solve this problem we are going to use the
Henderson-Hasselbach equation and clear for the molar ratio. Keep in mind that we need the value for Acetic Acid's pKa, which can be found in tables and is
4,76:
![pH=pKa + log ( \frac{[CH_3COONa]}{[CH_3COOH]} )](https://tex.z-dn.net/?f=pH%3DpKa%20%2B%20log%20%28%20%5Cfrac%7B%5BCH_3COONa%5D%7D%7B%5BCH_3COOH%5D%7D%20%29%20)
![\frac{[CH_3COOH]}{[CH_3COONa}= 10^{(pH-pKa)^{-1}}=10^{(4-4,76)^{-1}}=5,75](https://tex.z-dn.net/?f=%20%5Cfrac%7B%5BCH_3COOH%5D%7D%7B%5BCH_3COONa%7D%3D%2010%5E%7B%28pH-pKa%29%5E%7B-1%7D%7D%3D10%5E%7B%284-4%2C76%29%5E%7B-1%7D%7D%3D5%2C75%20)
So, the mole ratio of CH₃COOH to CH₃COONa is
5,75Have a nice day!
Ionized, become charged, become a cation
hopefully that helps
Answer:
CN^- is a strong field ligand
Explanation:
The complex, hexacyanoferrate II is an Fe^2+ specie. Fe^2+ is a d^6 specie. It may exist as high spin (paramagnetic) or low spin (diamagnetic) depending on the ligand. The energy of the d-orbitals become nondegenerate upon approach of a ligand. The extent of separation of the two orbitals and the energy between them is defined as the magnitude of crystal field splitting (∆o).
Ligands that cause a large crystal field splitting such as CN^- are called strong field ligands. They lead to the formation of diamagnetic species. Strong field ligands occur towards the end of the spectrochemical series of ligands.
Hence the complex, Fe(CN)6 4− is diamagnetic because the cyanide ion is a strong field ligand that causes the six d-electrons present to pair up in a low spin arrangement.
Answer:
umm.. B. a base that generates a lot of hydroxide ions in water.
