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2. Zaytsev's rule - Wikipedia

   en.wikipedia.org/wiki/Zaytsev's_rule

   More generally, Zaytsev's rule predicts that in an elimination reaction the most substituted product will be the most stable, and therefore the most favored. The rule makes no generalizations about the stereochemistry of the newly formed alkene, but only the regiochemistry of the elimination reaction. While effective at predicting the favored ...

3. Addition reaction - Wikipedia

   en.wikipedia.org/wiki/Addition_reaction

   In organic chemistry, an addition reaction is an organic reaction in which two or more molecules combine to form a larger molecule called the adduct. [1] [2] An addition reaction is limited to chemical compounds that have multiple bonds. Examples include a molecule with a carbon–carbon double bond (an alkene) or a triple bond (an alkyne).

4. Alkene - Wikipedia

   en.wikipedia.org/wiki/Alkene

   Alkenes react with percarboxylic acids and even hydrogen peroxide to yield epoxides: RCH=CH 2 + RCO 3 H → RCHOCH 2 + RCO 2 H. For ethylene, the epoxidation is conducted on a very large scale industrially using oxygen in the presence of silver-based catalysts: C 2 H 4 + 1/ 2 O 2 → C 2 H 4 O. Alkenes react with ozone, leading to the scission ...

5. Oxymercuration reaction - Wikipedia

   en.wikipedia.org/wiki/Oxymercuration_reaction

   In organic chemistry, the oxymercuration reaction is an electrophilic addition reaction that transforms an alkene (R 2 C=CR 2) into a neutral alcohol. In oxymercuration, the alkene reacts with mercuric acetate (AcO−Hg−OAc) in aqueous solution to yield the addition of an acetoxymercury (−HgOAc) group and a hydroxy (−OH) group across the ...

6. Transition metal alkene complex - Wikipedia

   en.wikipedia.org/wiki/Transition_metal_alkene...

   The barrier for the rotation of the alkene about the M-centroid vector is a measure of the strength of the M-alkene pi-bond. Low symmetry complexes are suitable for analysis of these rotational barriers associated with the metal-ethene bond.In Cp Rh(C 2 H 4 )(C 2 F 4 ), the ethene ligand is observed to rotate with a barrier near 12 kcal/mol but ...

7. Hydroformylation - Wikipedia

   en.wikipedia.org/wiki/Hydroformylation

   Hydroformylation of an alkene (R 1 to R 3 organyl groups (i. e. alkyl-or aryl group) or hydrogen). In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from alkenes (R 2 C=CR 2).

8. NYT ‘Connections’ Hints and Answers Today, Thursday ... - AOL

   www.aol.com/nyt-connections-hints-answers-today...

   Get ready for all of today's NYT 'Connections’ hints and answers for #585 on Thursday, January 16, 2025. Today's NYT Connections puzzle for Thursday, January 16, 2025 The New York Times

9. Wilkinson's catalyst - Wikipedia

   en.wikipedia.org/wiki/Wilkinson's_catalyst

   Wilkinson's catalyst also catalyzes many other hydrofunctionalization reactions including hydroacylation, hydroboration, and hydrosilylation of alkenes. [14] Hydroborations have been studied with catecholborane and pinacolborane. [15] It is also active for the hydrosilylation of alkenes. [16]