As far as I run, I never mee...
[4559] As far as I run, I never mee... - As far as I run, I never meet my brother on my right. What am I? - #brainteasers #riddles - Correct Answers: 15 - The first user who solved this task is Manguexa Wagle
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As far as I run, I never mee...

As far as I run, I never meet my brother on my right. What am I?
Correct answers: 15
The first user who solved this task is Manguexa Wagle.
#brainteasers #riddles
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The Baloonist

A woman in a hot air balloon realized she was lost.
She reduced altitude and spotted a man below. She descended a bit more and shouted: 'Excuse me, can you help me? I promised a friend I would meet him an hour ago but I don't know where I am..'
The man below replied, 'You're in a hot air balloon hovering approximately 30 feet above the ground. You're between 40 and 41 degrees north latitude and between 59 and 60 degrees west longitude.'
'You must be an Engineer,' said the balloonist.
'I am,' replied the man, 'how did you know?'
'Well,' answered the balloonist, 'everything you have told me is probably technically correct, but I've no idea what to make of your information and the fact is, I'm still lost. Frankly, you've not been much help at all. If anything, you've delayed my trip by your talk.'
The man below responded, 'You must be in Management.'
'I am,' replied the balloonist, 'but how did you know?'
'Well,' said the man, 'you don't know where you are or where you're going. You have risen to where you are, due to a large quantity of hot air. You made a promise, which you've no idea how to keep, and you expect people beneath you to solve your problems. The fact is you are in exactly the same position you were in before we met, but now, somehow, it's my f**king fault.'

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Kurt Alder

Died 20 Jun 1958 at age 55 (born 10 Jul 1902).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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