Answer:
melting point will be higher than that of pure ethyl acetate
Explanation:
Answer: (Structure attached).
Explanation:
This type of reaction is an aromatic electrophilic substitution. The overall reaction is the replacement of a proton (H +) with an electrophile (E +) in the aromatic ring.
The aromatic ring in p-fluoroanisole has two sustituents, an <u>halogen</u> and a <u>methoxy group</u>, which are <em>ortho-para</em> directing substituents.
Aryl sulfonic acids are easily synthesized by an electrophilic substitution reaction aromatic using <u>sulfur trioxide as an electrophile</u> (very reactive).
The reaction occurs in three steps:
- The attack on the electrophile forms the sigma complex.
- The loss of a proton regenerates an aromatic ring.
- The sulfonate group can be protonated in the presence of a strong acid (H₂SO₄).
Normally, a mixture of <em>ortho-para</em> substituted products would be obtained. However, since both <em>para</em> positions are occupied, only the <em>ortho </em>substituted product is obtained here.
Dipole interactions are observed in covalent bonds. In ionic bonding, permanent transfer of electrons occurs and due to this dipole-dipole interactions are not observed. In covalent bonding, electron cloud is shared between 2 atoms. If this electron cloud is not shared equally between them, polarities are formed in a molecule. And hence we say that the molecule is polar. For a molecule to be polar, there should be electronegativity difference between them. Atom with greater electronegative attracts electron cloud more towards itself whereas atom with lesser electronegative attracts electron cloud less. But there is no permanent transfer of electrons. Due to this electronegativity differences, atom with more electronegative gains partial negative charge and atom with lesser electronegative value gains partial positive charge. The charge is partial because there is no complete transfer of electrons.
Answer:
the reaction will come to a halt and the other reactant will still be present.
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