Answer:
% (COOK)2H2O = 37.826 %
Explanation:
mix: (COOK)2H2O + Ca(OH)2 → CaC2O4 + H2O
∴ mass mix = 4.00 g
∴ mass (CaC2O4)H2O = 1.20 g
∴ Mw (COOK)2H2O = 184.24 g/mol
∴ Mw (CaC2O4)H2O = 146.12 g/mol
∴ r = mol (COOK)2H2O / mol (CaC2O4)H2O = 1
- % (COOK)2H2O = (mass (COOK)2H2O / mass Mix) × 100
⇒ mass (COOK)2H2O = (1.20 g (CaC2O4)H2O)×(mol (CaC2O4)H2O / 146.12 g (CaC2O4)H2O)×(mol (COOK)2H2O/mol (CaC2O4)H2O)×(184.24 g (COOK)2H2O/mol (COOK)2H2O)
⇒ mass (COOK)2H2O = 1.513 g
⇒ % (COOK)2H2O = ( 1.513 g / 4 g )×100
⇒ % (COOK)2H2O = 37.826 %
Answer:
Sodio (Na), elemento químico del grupo de los metales alcalinos (Grupo 1 [Ia]) de la tabla periódica. El sodio es un metal blanco plateado muy suave. El sodio es el metal alcalino más común y el sexto elemento más abundante en la Tierra, y comprende el 2,8 por ciento de la corteza terrestre.
Explanation:
Espero que esto ayude a marcar el MÁS CEREBRAL !!!
Time Period 3 (300 BC to 1400 AD)
The alchemists were in pursuit of 2 ideals. First, alchemy came about from the belief that cheap metals can be transmuted to gold using the legendary substance <em>Philosopher's Stone</em> for the conversion. These views were greatly influenced by Aristotle. Thus, from 300 BC to 1400 AD, alchemists worked to make the conversion of cheap metals to gold a reality. However, it never succeeded.
After this, the second ideal that the alchemists were in pursuit of was the concoction of an elixir of life to enable people to live longer and cure all ailments. This took place in the 1500s up to the end of the 1600s. Just like the pursuit of the first ideal, efforts to succeed in the second one all led to failure.
PV=nRT
You are funding pressure and you have V = 9.45L, n = 1.9 moles, R = gas constant, and T = 228 K
P(9.45L) = (1.9moles)(0.0821)(228K)
Find P
Multiply
9.45P = 35.57
Divide
P = 3.76 L of N
Answer should be 3.76 liters of nitrogen
Explanation:
Dehydrohalogenation reactions occurs as elimination reactions through the following mechanism:
Step 1: A strong base(usually KOH) removes a slightly acidic hydrogen proton from the alkyl halide.
Step 2: The electrons from the broken hydrogen‐carbon bond are attracted toward the slightly positive carbon (carbocation) atom attached to the chlorine atom. As these electrons approach the second carbon, the halogen atom breaks free.
However, elimination will be slower in the exit of Hydrogen atom at the C2 and C3 because of the steric hindrance by the methyl group.
Elimination of the hydrogen from the methyl group is easier.
Thus, the major product will A