PALINDROME
[1989] PALINDROME - Make the palindrome of the following letters: A, A, A, A, A, A, A, A, C, C, E, E, E, E, F, F, L, L, M, M, N, N, O, O, O, O, O, O, O, O, R, R, R, R, R, R, T, T, W, W, Y, Y, Y, Y - #brainteasers #wordpuzzles #palindrome - Correct Answers: 29 - The first user who solved this task is Neelima Subrahmanyam
BRAIN TEASERS
enter your answer and press button OK

PALINDROME

Make the palindrome of the following letters: A, A, A, A, A, A, A, A, C, C, E, E, E, E, F, F, L, L, M, M, N, N, O, O, O, O, O, O, O, O, R, R, R, R, R, R, T, T, W, W, Y, Y, Y, Y
Correct answers: 29
The first user who solved this task is Neelima Subrahmanyam.
#brainteasers #wordpuzzles #palindrome
Register with your Google Account and start collecting points.
Check your ranking on list.

Soap And Water

After several exciting dates, Jim invited Tina over to his house for a home-cooked dinner.
When she sat down at the table, she noticed that the dishes were the dirtiest that she had ever seen in her life.
"Have these dishes ever been washed?" Tina asked, running her fingers over the grit and grime.
Jim replied, "They're as clean as soap and water could get them."
Tina felt a bit apprehensive, but started eating. It was really delicious and she said so, despite the dirty dishes.
When dinner was over, Jim took the dishes outside, whistled and yelled, "Here, Soap! Here, Water!"

Jokes of the day - Daily updated jokes. New jokes every day.
Follow Brain Teasers on social networks

Brain Teasers

puzzles, riddles, mathematical problems, mastermind, cinemania...

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.
This site uses cookies to store information on your computer. Some are essential to help the site properly. Others give us insight into how the site is used and help us to optimize the user experience. See our privacy policy.