Do anyone know how to do question B
1 answer:
Answer:
a) IUPAC Names:
1) (<em>trans</em>)-but-2-ene
2) (<em>cis</em>)-but-2-ene
3) but-1-ene
b) Balance Equation:
C₄H₁₀O + H₃PO₄ → C₄H₈ + H₂O + H₃PO₄
As H₃PO₄ is catalyst and remains unchanged so we can also write as,
C₄H₁₀O → C₄H₈ + H₂O
c) Rule:
When more than one alkene products are possible then the one thermodynamically stable is favored. Thermodynamically more substituted alkenes are stable. Furthermore, trans alkenes are more stable than cis alkenes. Hence, in our case the major product is trans alkene followed by cis. The minor alkene is the 1-butene as it is less substituted.
d) C is not Geometrical Isomer:
For any alkene to demonstrate geometrical isomerism it is important that there must be two different geminal substituents attached to both carbon atoms. In 1-butene one carbon has same geminal substituents (i.e H atoms). Hence, it can not give geometrical isomers.
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Answer:
See explanation
Explanation:
The synthesis of aspirin is shown in the reaction scheme attached to this answer. The production of aspirin involves the reaction of acetyl salicyclic acid and acetic anhydride. HA in the reaction mechanism refers to an acid that is used in the reaction
Similarly benzamide, is converted to the carbonyl carbocation by reaction with acid. The -NH2 group is protonated and subsequently departs as a leaving group. An OH^- completes the mechanism forming a carboxylic acid. The movement of electrons is shown in the image attached.
Again, the diazotization of benzamide using sodium nitrate and concentrated HCl yields benzene diazonium chloride. Addition of water to benzene diazonium chloride yields the benzoic acid and nitrogen gas.
