For every 1 mole of C6H12O6, you need 6 moles of water. Multiply the 2.5 moles you are trying to make by the 6 of water you need, and 4) 15 is your answer.
I really hope that this helps. H-F because the difference in electronegativity is the greatest, about 1.9 on the Pauling scale. The term means which bond has the greatest polarity and is thus most similar to an ionic bond, which involves the transfer of an electron (in opposition to covalent bonds, which share electrons). It is H-F because out of all the atoms here bonded with H, ie hydrogen, F is the most electronegative which means it can pull the bonded electrons to itself more than can Cl, O, and N. <span>That means a stronger polarization of the electron cloud forming the bond with hydrogen and therefore a stronger ionic character.</span>
Answer:
Explanation:
Given parameters:
Molarity of KOH = 0.26M
Volume of H₂SO₄ = 19.76mL
Molarity of H₂SO₄ = 0.20M
Unknown:
Volume of KOH = ?
Solution:
This is a neutralization reaction in which an acid reacts with a base to produce salt and water:
H₂SO₄ + 2KOH → K₂SO₄ + 2H₂O
We solve from the known to the unknown in the reaction.
The known is the acid and from there we can find the number of moles of the acid to be completely neutralized:
Number of moles of acid = molarity x volume
Number of moles of acid = 19.76 x 0.20 = 3.95mol
From the balanced reaction equation:
1 mole of acid reacts with 2 moles of the bases KOH
3.95mole of acid would react with 3.95moles x 2 of the base
Number of moles of reacting base = 7.90moles
To find the volume of base;
Volume of base = 
Volume =
= 30.40mL
Learn more:
Neutralization brainly.com/question/6447527
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2-bromo-1-chloro-4-nitrobenzene is being synthesized in following sequence:
Step 1: Chlorination of Benzene:
This is Halogenation reaction of benzene. In this step benzene is reacted with Chlorine gas in the presence of lewis acid (i.e. FeCl₃). This results in the formation of Chlorobenzene as shown in red step below.
Step 2: Nitration of Chlorobenzene:
The chlorine atom on benzene has a ortho para directing effect. Therefore, the nitration of chlorobenzene will yield para nitro chlorobenzene as shown in blue step below.
Step 3: Bromination of 1-chloro-4-nitrobenzene:
In this step bromination is done by reacting bromine in the presence of lewis acid. The chlorine being ortho para directing in nature and nitro group being meta directing in nature will direct the incoming Br⁺ (electrophile) to the desired location. Hence, 2-bromo-1-chloro-4-nitrobenzene is synthesized in good yield.