Top Posters
Since Sunday
5
a
5
k
5
c
5
B
5
l
5
C
4
s
4
a
4
t
4
i
4
r
4
New Topic  
tlcone72 tlcone72
wrote...
Posts: 24
Rep: 0 0
11 years ago
This one for example, what reagents do I use?

http://oi46.tinypic.com/2lw38sx.jpg
Read 1184 times
3 Replies
Replies
tlk
wrote...
11 years ago
H2/Lindlar
wrote...
11 years ago
You must have the gas in contact with a Lindlar's Catalyst.
Lindlar's Catayst produces a cis-alkene.

A Lindlar's Catalyst is a Palladium that is poisoned with lead and CaCo3
Palladium usually turns an alkyne into an alkane.
But the Lindlar's catalyst can contaminate your sample with poisonous lead.

That is probably the easiest & inexpensive way to make a cis-alkene.
cis-alkenes are very hard to produce and needed a contact catalyst.
You may as well find a replacement for a Lindlar's Catalyst.
There are some ChemLab suppliers that claim to have a better alternative for the Lindlar's Catalyst.
Answer accepted by topic starter
tlaskeytlaskey
wrote...
Posts: 14
Rep: 1 0
11 years ago
Sign in or Sign up in seconds to unlock everything for free
This verified answer contains over 120 words.
1

Related Topics

New Topic      
Explore
Post your homework questions and get free online help from our incredible volunteers
  1243 People Browsing
Related Images
  
 128
  
 807
  
 4430
Your Opinion
Which country would you like to visit for its food?
Votes: 204