Chess Knight Move
[4029] Chess Knight Move - Find the country and its capital city, using the move of a chess knight. First letter is M. Length of words in solution: 10,10. - #brainteasers #wordpuzzles #chessknightmove - Correct Answers: 30 - The first user who solved this task is Manguexa Wagle
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Chess Knight Move

Find the country and its capital city, using the move of a chess knight. First letter is M. Length of words in solution: 10,10.
Correct answers: 30
The first user who solved this task is Manguexa Wagle.
#brainteasers #wordpuzzles #chessknightmove
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The runner

Mary was having an affair during the day while her husband was at work. One day, she was in bed with her boyfriend Ralph, when she heard her husband's car pull in the driveway. She yelled at Ralph, "Hurry! grab your clothes and jump out the window, my husband is home early!"

Ralph looked out the window and said, "I can't jump out the window! It's raining like hell out there."

Mary cried, "If my husband catches us in here, he will kill both of us!"

So, Ralph grabbed his clothes and jumped out the window. When he landed outside he found himself in the middle of a marathon race, so he started running along side the others, only he was still in the nude, carrying his clothes on his arm.

One of the runners asked him, "Do you always run in the nude?"

Ralph answered, while gasping for air, "Oh yes, it feels so free having the air blow over your skin while you are running."

Then another runner asked, "Do you always run carrying your clothes on your arm?"

Ralph answered breathlessly, "Oh yes, that way I can get dressed at the end of the run and get in my car to go home."

Then another runner asked, "Do you always wear a condom when you run?"

Ralph answered, "Only if it's raining."

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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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