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Chemistry
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claws
  • Member for 12 years, 2 months
  • Last seen more than 1 year ago
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Top posts
question
22
Why do Organolithium or Grignard reagents act as nucleophiles and not as bases with aldehydes and ketones
Jan 18, 2013
question
20
How do the molecules know the future? How do they proceed to form "Most Stable" compound?
Jan 20, 2013
question
14
What will be the product when 3,4-dibromocyclohexene is reacted with sodium followed by heating with selenium?
Jan 14, 2013
question
10
What would be the mechanism of the given reaction?
Jan 14, 2013
question
9
Why are carbonyl compunds more reactive towards catalytic hydrogenation than alkynes and alkenes?
Jan 14, 2013
question
6
What will be the major product of of the Wurtz reaction of 3,6-dibromocyclohexa-1,4-diene?
Jan 14, 2013
question
4
What will be the Ozonolysis product?
Jan 14, 2013
question
2
Can bromide ion ever act like a base?
Jan 18, 2013
Top network posts
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1354
Making sense of principal component analysis, eigenvectors & eigenvalues
1109
What is the meaning of "POSIX"?
822
What is an application binary interface (ABI)?
772
What is Common Gateway Interface (CGI)?
305
What are the calling conventions for UNIX & Linux system calls (and user-space functions) on i386 and x86-64