Waves that require a medium through which to travel are electromagnetic waves. True or False?
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The organic product formed when 1−hexyne is treated with H₂O, H₂SO₄, and HgSO₄ will be 2-hexanone (structure attached).
This reaction is an example of an oxymercuration reaction of the organic product 1−hexyne.
Oxymercuration is shown in three steps to the right. The nucleophilic double bond attacks the mercury ion, releasing an acetoxy group. The mercury ion's electron pair attacks carbon on the double bond, generating a positive-charged mercuronium ion. Mercury's dxz and 6s orbitals give electrons to the double bond's lowest unoccupied molecular orbitals.
In the second stage, the nucleophilic H₂O attacks the highly modified carbon, freeing its mercury-bonding electrons. Electrons neutralize mercury ions by collapsing. Water molecules have positive-charged oxygen.
In the third stage, the negatively charged acetoxy ion released in the first step attacks the hydrogen of the water group, generating the waste product HOAc. The two electrons in the oxygen-hydrogen link collapse into oxygen, neutralizing its charge and forming alcohol.
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Answer:
1,4-hexanediamine contains two functional groups.
Explanation:
1,4-hexanediamine is an organic molecule which contains two functional groups at C-1 and C-4 position.
The longest carbon chain in 1,4-hexanediamine contains six carbon atoms.
Molecular formula of 1,4-hexanediamine is .
1,4-hexanediamine used as a bidentate ligand in organometallic chemistry.
The structure of 1,4-hexanediamine is shown below.
