My dress is tranquil when I ...
[5212] My dress is tranquil when I ... - My dress is tranquil when I tread the earth, or dwell at home, or drift on the water. Sometimes my wings and this wide sky lift me over the dwellings of men, and then strong clouds carry me over the people. My ornaments echo loudly and melodiously, Illustriously sing when I am not near the earth and stream, a sailing spirit. What am I? - #brainteasers #riddles - Correct Answers: 26 - The first user who solved this task is Djordje Timotijevic
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My dress is tranquil when I ...

My dress is tranquil when I tread the earth, or dwell at home, or drift on the water. Sometimes my wings and this wide sky lift me over the dwellings of men, and then strong clouds carry me over the people. My ornaments echo loudly and melodiously, Illustriously sing when I am not near the earth and stream, a sailing spirit. What am I?
Correct answers: 26
The first user who solved this task is Djordje Timotijevic.
#brainteasers #riddles
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A lawyer calls a plumber for help...

The plumber assesses the situation and says, "I can fix it today for $800."

The lawyer, surprised, asks, "How long will it take?" The plumber replies, "I'll need about an hour to get a part from the supply house and another hour to do the repair."

The lawyer, smirking, says, "Two hours for $800? That's $400 per hour! I'm a lawyer, and I charge $350 per hour!"

The plumber nods and says, "Yes, I understand. That's why I left my law practice."

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Kurt Alder

Born 10 Jul 1902; died 20 Jun 1958 at age 55.German chemist was the corecipient (with Otto Diels) of the Nobel Prize for Chemistry in 1950 for their development of the Diels-Alder reaction (1928), or diene synthesis, a widely used method of synthesizing cyclic organic compounds. In this type of reaction, a compound containing two double bonds separated by a single bond (i.e. a conjugated diene) adds to a suitable compound containing one double bond (dienophile) to give a ring compound. In the dienophile, the double bond must have a carbonyl group on each side. The reaction proceeds in the mildest conditions, is of general application, and hence of great utility in synthesis. It is used in the synthesis of natural products, such as sterols, vitamin K, cantharides, and synthetic polymers.
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