Answer:
CH₃CH₂CH₂COOH > CH₃CH₂COOH > ClCH₂CH₂COOH > ClCH₂COOH
Explanation:
Electron-withdrawing groups (EWGs) increase acidity by inductive removal of electrons from the carboxyl group.
Electron-donating groups (EDGs) decrease acidity by inductive donation of electrons to the carboxyl group.
- The closer the substituent is to the carboxyl group, the greater is its effect.
- The more substituents, the greater the effect.
- The effect tails off rapidly and is almost zero after about three C-C bonds.
CH₃CH₂-CH₂COOH — EDG — weakest — pKₐ = 4.82
CH₃-CH₂COOH — reference — pKₐ = 4.75
ClCH₂-CH₂COOH — EWG on β-carbon— stronger — pKₐ = 4.00
ClCH₂COOH — EWG on α-carbon — strongest — pKₐ = 2.87
<span><span>When you write down the electronic configuration of bromine and sodium, you get this
Na:
Br: </span></span>
<span><span />So here we the know the valence electrons for each;</span>
<span><span>Na: (2e)
Br: (7e, you don't count for the d orbitals)
Then, once you know this, you can deduce how many bonds each can do and you discover that bromine can do one bond since he has one electron missing in his p orbital, but that weirdly, since the s orbital of sodium is full and thus, should not make any bond.
However, it is possible for sodium to come in an excited state in wich he will have sent one of its electrons on an higher shell to have this valence configuration:</span></span>
<span><span /></span><span><span>
</span>where here now it has two lonely valence electrons, one on the s and the other on the p, so that it can do a total of two bonds.</span><span>That's why bromine and sodium can form </span>
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Answer:
they are producers and they have means to keep themselves warm
Explanation:
I took test and saw answer.
