Answer:
Explanation:
Polar molecules interact with other molecules of similar polarity to form solutions. Non-polar molecules do not interact the same way.
pH of the solution after 24. 00 ml of the hcl has been added is 12.87
millimoles NaOH = mL x M = 24.00 mL x 0.25 M = 6.00
millimoles HCl = 24.00 mL x 0.10 M = 2.40
total volume = 48.00 mL
.................................NaOH + HCl ==>NaCl + H2O
initial.........................6.00.........0............0.........0
added.....................................2.40............................
change.................... -2.40......-2.40.........+2.40.... +2.40
equilibrium.................3.60.........0..............2.40.......2.40
The NaCl contributes nothing to the pH of the final solution. The pH is determined by the excess of NaOH present. (NaOH) = millimoles/mL = 3.60/48.00 = 0.075 M = (OH^-)
pOH = -log (OH^-). Then
pOH = -log (0.075)
pOH =1.1249
As we know,
pH + pOH = pKw = 14.00
pH=14-pOH
pH=14-1.1249
pH=12.87
<h3>
What is pH?</h3>
pH is a logarithmic measure of an aqueous solution's hydrogen ion concentration. pH = -log[H+], where log is the base 10 logarithm and [H+] is the concentration of hydrogen ions in moles per liter.
The pH of an aqueous solution describes how acidic or basic it is, with a pH less than 7 being acidic and a pH greater than 7 being basic. A pH of 7 is regarded as neutral (e.g., pure water). pH values typically range from 0 to 14, though very strong acids may have a negative pH and very strong bases may have a pH greater than 14.
Learn more about pH:
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Answer:
Wood
Explanation:
It is because sound is a longitudinal wave
Answer:
which answer questions hi to nhi hai
Many electrophilic aromatic halogenations require the presence of an aluminum trihalide as a catalyst. We generally acetylated the amino group as protection. Now, this acetanilide can be brominated at Ortho or para position. An atom that is attached to an aromatic system usually hydrogen is replaced by an electrophile is an organic reaction which is called Electrophilic aromatic substitution. There are what you called important electrophilic aromatic substitutions they are aromatic nitration, aromatic sulfonation, aromatic halogenation and acylation and alkylating Friedel-Crafts reaction. Aromatic bromination is an electrophilic aromatic substitution (EAS) reaction, which will require benzene to act as a nucleophile to acquire an electrophile. Therefore, any directing groups that activate the ring will make it react more quickly with respect to aromatic bromination. Acetanilide is a moderately-activated ring <span>having a decent EWG.</span>
