Why is this organic Salt soluble in a high acidic concentration

Started by Sanskrit | Last post by Sanskrit October 09, 2013, 01:44:47 PM

Why is this reaction SN2?

Started by limonade | Last post by Babcock_Hall March 16, 2013, 12:01:14 PM

Why Is This the Major Product (Nucleophilic Substitution/Eliminiation)

Started by MetsFan09 | Last post by MetsFan09 October 13, 2010, 03:33:53 PM

Why isn't BF3 a nucleophile?

Started by Manchi0528 | Last post by chenbeier October 16, 2018, 06:55:26 AM

Why isn't cis-stilbene favoured?

Started by brettlawrie | Last post by orgopete February 26, 2012, 10:08:51 AM

Why isn't NaH used for carbonyl reduction?

Started by chiddler | Last post by Mobius1988 March 02, 2012, 08:42:49 PM

Why isn't these identical and optically inactive molecules?

Started by tangent1.57 | Last post by thfmag August 05, 2009, 05:03:43 PM

why it is?

Started by tortoise | Last post by Yggdrasil December 25, 2006, 07:22:32 PM

Why it's not possible for both rings on naphthalene to be benzenoid at same time

Started by AussieKenDoll | Last post by Enthalpy July 16, 2019, 03:41:30 AM

Why m-xylene?

Started by Pranav « 1 2 » | Last post by curiouscat January 08, 2013, 01:43:30 AM

why more nucleophilic reactants ==> faster reaction?

Started by iScience | Last post by clarkstill December 13, 2013, 02:53:25 AM

Why must a stopper at the top of the seperatory funnel be removed before liquid

Started by bamster | Last post by pacifyer April 06, 2010, 02:31:26 PM

why nacl is used in 1-butanol to 1-bromobutane reaction

Started by uracowman | Last post by cyclotomamine July 09, 2009, 02:42:18 AM

Why no alt. Tosylates to OTf for replacement of Halide in Pd cat. cross coupling

Started by Cheese_Burgers | Last post by Cheese_Burgers August 08, 2014, 10:25:41 AM

Why no direct displacement at SP2 carbons?

Started by spirochete | Last post by kryptoniitti May 12, 2008, 04:15:32 PM