RCN + SnCl2 + HCl → RCH = NH H2 +ORCHO This reaction is called Stephen reaction.
A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
Why do we use SnCl2 in the Stephen reaction? - Quora
Stephen Reaction Mechanism, Stephen Aldehyde Synthesis Mechanism Explanation
organic chemistry - Nitrobenzene reduction with (tin) Sn catalyst: Why is C-H bond cleavage preferred over O-H bond cleavage? - Chemistry Stack Exchange
Scheme 1. Reagents and conditions: (a) NaNO2, HCl, SnCl2, -5 ⁰C to RT,... | Download Scientific Diagram
Tin(II) chloride
A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
File:SnCl2 Stephen reduction.svg - Wikimedia Commons
Scheme 1. Reagents and conditions: (a) NaNO2, HCl, SnCl2, -5 ⁰C to RT,... | Download Scientific Diagram
What's the mechanism for the reduction of aromatic nitro group when using Fe and NH4Cl?
Catalyst SnCl(2)//HCl is used in
Tin(II) chloride - Wikipedia
organic chemistry - Does this reduction mechanism of an diazonium via stannic chloride sense? - Chemistry Stack Exchange
Tin(II) chloride - Wikipedia
Reduction of Nitro Groups, The Baeyer-Villiger, and Protection of Amines
![The reaction RCN [ ]SnCl2/HCl (A) [ ]H2O RCHO + NH4Cl is known as:](https://d1hj4to4g9ba46.cloudfront.net/questions/1645507_1780626_ans_cfe45c9ca8fe42bd9c9eb464a1a38714.png "The reaction RCN [ ]SnCl2/HCl (A) [ ]H2O RCHO + NH4Cl is known as:")
The reaction RCN [ ]SnCl2/HCl (A) [ ]H2O RCHO + NH4Cl is known as:
Reduction of Nitro Groups, The Baeyer-Villiger, and Protection of Amines
Tin(ii) chloride assisted synthesis of N -protected γ -amino β -keto esters through semipinacol rearrangement - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C0OB00199F
A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
Why do we use SnCl2 in the Stephen reaction? - Quora
Solved Hi i am very confused with this please help by | Chegg.com
Stephen Reaction Mechanism, Stephen Aldehyde Synthesis Mechanism Explanation
Why do we use SnCl2 in the Stephen reaction? - Quora
Synthesis of 2,5-disubstitued benzimidazole using SnCl2-catalyzed reduction system at room temperature - ScienceDirect
Solved How do you complete the second step which is | Chegg.com
