Answer:
a fluid
Explanation:
in which the viscous stresses arising from its flow, at every point, are linearly correlated to the local strain rate—the rate of change of its deformation over time.
Answer:
This reaction is an hydration of alkenes and the major product is 3-ethyl-2-heptanol
Explanation:
In this reaction in the first step water is the nuclophile and the alkene is the electrophile. Then, the carbanion is the nucleophile and attacks a proton from the water forming the respective alcohol. This carbanionic compound is a reaction intermediary. You can see the mechanism in the picture.
Is that carbanionic compound who explained the major product because the more substituted carbanion the most stable intermediary. Thus, the 3-ethyl-2-heptanol intermediary is the most stable and this product is the major one.
I hope it helps!
Answer:
i think A but im not sure
Explanation: