Answer:
Decrease temperature or reduce pressure
Washes and extractions are both techniques that use a separatory funnel to separate liquid layers. However, washes and extractions have differences. Determine whether each statement applies to washes or extractions.
Leaves impurities in their starting layer Choose...
Moves impurities from one layer to another Choose...
Moves desired compound from one layer to another Choose...
Often involves a reaction in one of the layers Choose...
Leaves desired compound in its starting layer Choose...
Answer:
Leaves impurities in their starting layer - Extraction Moves impurities from one layer to another - Wash Moves desired compound from one layer to another - Extraction Often involves a reaction in one of the layers - Extraction Leaves desired compound in its starting layer - WashExplanation:
Both extraction and wash are technical materials separation processes. Both seek to carry out a separation of liquid-liquid, through the relationship between solvent and solute present in this solution. Both use a separation funnel and are very similar processes where the main difference is the purpose that each one seeks to exercise. The extraction causes the dissolution of the material that the researcher wants to leave behind. this process leaves impurities in the initial solution layer and moves the researcher's desired compound to the second layer of solution. A chemical reaction can take place during this process.
A wash, on the other hand, dissolves all impurities from the solution and extracts the compound desired by the researcher. Therefore, we can conclude that during this process the impurities are moved from one layer to another in the solution until it is discarded from the funnel, leaving the desired compound in the initial layer.
In the electrolysis of water, how long will it take to produce 75.00 L of H2 at 1.0 atm and 273 K using an electrolytic cell through which the current is 205.0 mA
answer is 2546 h
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Why does glucose and acentic acid have the same empirical formula
Answer:
Examples. Glucose (C6H12O6), ribose (C5H10O5), Acetic acid (C2H4O2), and formaldehyde (CH2O) all have different molecular formulas but the same empirical formula: CH2O.
Explanation:In chemistry, the empirical formula of a chemical compound is the simplest positive integer ratio of atoms present in a compound.
Naturally occurring gallium is a mixture of isotopes
that contains 90.11% of Ga-69 (atomic mass = 68.93
u) and 9.89% of Ga-71 (atomic mass 70.92 u).
What is the average atomic mass of naturally
occurring gallium?
A) 69.93 amu
C) 69.50 amu
B) 69.12 amu
D) 69.00 amu
You are given a solution containing a pair of enantiomers (A and B). Careful measurements show that the solution contains 98% A and 2% B. What is the ee of this solution
Answer:
ee = 96%
Explanation:
Enantiomeric excess, ee, is a way to express a mixture that is not enantiomerically pure. It is defined as 100 times the ratio between the differences of amounts of enantiomers and the total amunt. that is:
ee = |A-B|/ A+B * 100
ee = |98%-2%| / 98+2 * 100
ee = 96%Phenols do not exhibit the same pka values as other alcohols; they are generally more acidic. Using the knowledge that hydrogen acidity is directly related to the stability of the anion formed, explain why phenol is more acidic than cyclohexane
Answer:
Phenols do not exhibit the same pka values as other alcohols;
They are generally more acidic.
Using the knowledge that hydrogen acidity is directly related to the stability of the anion formed, explain why phenol is more acidic than cyclohexane.
Explanation:
According to Bromsted=Lowry acid-base theory,
an acid is a substance that can release [tex]H^{+}[/tex] ions when dissolved in water.
So, acid is a proton donor.
If the conjugate base of an acid is more stable then, that acid is a strong acid.
In the case of phenol,
the phenoxide ion formed is stabilized by resonance.
[tex]C_6H_5OH -> C_6H_5O^- +H^+[/tex]
The resonance in phenoxide ion is shown below:
Whereas in the case of cyclohexanol resonance is not possible.
So, cyclohexanol is a weak acid compared to phenol.
