![Reagents and conditions: (a) i) NaNO2, H2O, TFA, 0°C; ii) NaN3, H2O,... | Download Scientific Diagram Reagents and conditions: (a) i) NaNO2, H2O, TFA, 0°C; ii) NaN3, H2O,... | Download Scientific Diagram](https://www.researchgate.net/publication/250926008/figure/fig4/AS:202611660726286@1425317792945/Reagents-and-conditions-a-i-NaNO2-H2O-TFA-0C-ii-NaN3-H2O-0C-to-room-temp.png)
Reagents and conditions: (a) i) NaNO2, H2O, TFA, 0°C; ii) NaN3, H2O,... | Download Scientific Diagram
![Decade Advances of NaN3 in Three‐component Reactions - Wang - 2023 - Asian Journal of Organic Chemistry - Wiley Online Library Decade Advances of NaN3 in Three‐component Reactions - Wang - 2023 - Asian Journal of Organic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/46cbc693-50c6-494a-945b-e124f0ec506c/ajoc202300105-fig-5010-m.jpg)
Decade Advances of NaN3 in Three‐component Reactions - Wang - 2023 - Asian Journal of Organic Chemistry - Wiley Online Library
![Copper-Catalyzed Azide–Alkyne Cycloaddition of Hydrazoic Acid Formed In Situ from Sodium Azide Affords 4-Monosubstituted-1,2,3-Triazoles | The Journal of Organic Chemistry Copper-Catalyzed Azide–Alkyne Cycloaddition of Hydrazoic Acid Formed In Situ from Sodium Azide Affords 4-Monosubstituted-1,2,3-Triazoles | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.1c02775/asset/images/medium/jo1c02775_0004.gif)
Copper-Catalyzed Azide–Alkyne Cycloaddition of Hydrazoic Acid Formed In Situ from Sodium Azide Affords 4-Monosubstituted-1,2,3-Triazoles | The Journal of Organic Chemistry
![SOLVED: 24-33 Predict the product(s) and provide the mechanism for each reaction below: (a) NaN3 + H2O, heat (b) NaN3 + 2H2O, heat (c) COCl2 + NaN3 + 2H2O, heat (d) NaN3 + 2H2O, heat SOLVED: 24-33 Predict the product(s) and provide the mechanism for each reaction below: (a) NaN3 + H2O, heat (b) NaN3 + 2H2O, heat (c) COCl2 + NaN3 + 2H2O, heat (d) NaN3 + 2H2O, heat](https://cdn.numerade.com/ask_images/7303982bd741463f8025f8b97188e7ca.jpg)
SOLVED: 24-33 Predict the product(s) and provide the mechanism for each reaction below: (a) NaN3 + H2O, heat (b) NaN3 + 2H2O, heat (c) COCl2 + NaN3 + 2H2O, heat (d) NaN3 + 2H2O, heat
![NaN3 → Product: H2O -NH2 only (b) (O)-NH, and HCOOH ca nu, only o O ENH: cod_OH + NH, NH2 (C) C-OH + NH3 NaN3 → Product: H2O -NH2 only (b) (O)-NH, and HCOOH ca nu, only o O ENH: cod_OH + NH, NH2 (C) C-OH + NH3](https://toppr-doubts-media.s3.amazonaws.com/images/4866555/d9fd1dc4-124d-456e-abb4-7189e12c7f7f.jpg)
NaN3 → Product: H2O -NH2 only (b) (O)-NH, and HCOOH ca nu, only o O ENH: cod_OH + NH, NH2 (C) C-OH + NH3
![SOLVED: 24-33 Predict the product(s) and provide the mechanism for each reaction below: (a) NaN3 + H2O, heat (b) NaN3 + 2H2O, heat (c) COCl2 + NaN3 + 2H2O, heat (d) NaN3 + 2H2O, heat SOLVED: 24-33 Predict the product(s) and provide the mechanism for each reaction below: (a) NaN3 + H2O, heat (b) NaN3 + 2H2O, heat (c) COCl2 + NaN3 + 2H2O, heat (d) NaN3 + 2H2O, heat](https://cdn.numerade.com/ask_previews/44d9146a-7f0b-40fb-aa61-f733d7bdaa65_large.jpg)
SOLVED: 24-33 Predict the product(s) and provide the mechanism for each reaction below: (a) NaN3 + H2O, heat (b) NaN3 + 2H2O, heat (c) COCl2 + NaN3 + 2H2O, heat (d) NaN3 + 2H2O, heat
![Solved) - A) op beste (CH3)2NH pH = 4.5 B) a Ime 2) NH2NH2, heat 1) NaN3 2)... (1 Answer) | Transtutors Solved) - A) op beste (CH3)2NH pH = 4.5 B) a Ime 2) NH2NH2, heat 1) NaN3 2)... (1 Answer) | Transtutors](https://files.transtutors.com/book/qimg/248abe69-c7aa-4e45-a9b6-1c685ec2f733.png)
Solved) - A) op beste (CH3)2NH pH = 4.5 B) a Ime 2) NH2NH2, heat 1) NaN3 2)... (1 Answer) | Transtutors
![Crystals | Free Full-Text | 5-Azido-4-dimethylamino-1-methyl-1,2,4-triazolium Hexafluoridophosphate and Derivatives Crystals | Free Full-Text | 5-Azido-4-dimethylamino-1-methyl-1,2,4-triazolium Hexafluoridophosphate and Derivatives](https://www.mdpi.com/crystals/crystals-06-00020/article_deploy/html/images/crystals-06-00020-g001.png)
Crystals | Free Full-Text | 5-Azido-4-dimethylamino-1-methyl-1,2,4-triazolium Hexafluoridophosphate and Derivatives
![Chiral Epoxides via Borane Reduction of 2-Haloketones Catalyzed by Spiroborate Ester: Application to the Synthesis of Optically Pure 1,2-Hydroxy Ethers and 1,2-Azido Alcohols | The Journal of Organic Chemistry Chiral Epoxides via Borane Reduction of 2-Haloketones Catalyzed by Spiroborate Ester: Application to the Synthesis of Optically Pure 1,2-Hydroxy Ethers and 1,2-Azido Alcohols | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo102294j/asset/images/large/jo-2010-02294j_0003.jpeg)