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.
Answer:
C. 1-ethyl, 3-methylcyclohexane
(Photo for proof at the bottom.)
Explanation:
The 1-ethyl is because you start numbering from the longest branch, towards the next closest branch. Prefix "eth-" means two, there are 2 carbons in the longest branch. 3-methyl is because the next branch is at number 3, and prefix "meth-" means 1, there is 1 carbon in that chain. "Cyclo" in cyclohexane means the skeletal model is shaped like a ring, and the "hexane" means there are 6 carbons in the ring. Prefix "hex" means 6.
Here's a photo of the unit review on Edge. Refer to the 2nd attachment for a visualization.
Please click the heart if this helped.
It's a chemical change because it's changing the object's property.
Calcium Floride (Caf2)
Hope this helped =D
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