Answer:
a) the minimun of acetic anhydride required for the reaction is 2.175 g (CH3CO)2O
b) V acetic anhydride = 2.010 mL
Explanation:
C6H4OHCOOH + (CH3CO)2O ↔ C9H8O4 + C2H4O2
⇒ mol salicylic acid = 2.94 g C6H4OHCOOH * ( mol C6H4OHCOOH / 138.121 g ) = 0.0213 mol C6H4OHCOOH
⇒ mol acetic anhydride = 0.0213 mol C6H4OHCOOH * ( mol (CH3CO)2O / mol C6H4OHCOOH ) = 0.0213 mol (CHECO)2O
⇒ g acetic anhydride = 0.0213 mol * ( 102.1 g/mol ) = 2.175 g CH3CO)2O
b) V = 2.175 g (CH3CO)2 * ( mL / 1.082 g ) = 2.010 mL (CH3CO)2O
The statement which is true is
Fluorine is more reactive than nitrogen because fluorine needs only one electron to fill its outermost shell.
<u><em>Explanation</em></u>
Fluorine has electron configuration of 1S²2S²2P⁵ while nitrogen has 1S²2S²2P³ electron configuration.
The 2P sub shell for nitrogen is half filled therefore it is sable than fluorine.
since p orbital can hold a maximum of 6 electrons ,Fluorine requires 1 electron to completely fill it's 2P sub shell which make it more reactive than nitrogen.
Answer:
(a) 
(b) 
Explanation:
Hello,
In this case, since the both gases behave ideally, with the given information we can compute the moles of He in A:

Thus, since the final pressure is 3.60 bar, we can write:

The moles of helium could be computed via solver as:

Or algebraically:

In such a way, the volume of the compartment B is:

Finally, he mole fraction of He is:

Regards.
In order to deprotonate an acid, we must remove protons in order to achieve a more stable conjugate base. For this example, we can use the relationship between carboxylic acid and hydroxide.
Deprotonation is the removal of a proton from a specific type of acid in reaction to its coming into contact with a strong base. The compound formed from this reaction is known as the conjugate base of that acid. The opposite process is also possible and is when a proton is added to a special kind of base. This is a process referred to as protonation, which forms the conjugate acid of that base.
For the example we have chosen to give, the conjugate base is the carboxylate salt. This would be the compound formed by the deprotonated carboxylic acid. The base in question was strong enough to deprotonate the acid due to the greater stability offered as a conjugated base.
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