![SOLVED: Predict the minor and major product DIPEA-diisopropylethylamina or Hunig s base DcJe malc prcducl rnE prcducl Predict products and indicate which one major product 4meducl ShowIne machansm oline lollowing reaclions Clearly SOLVED: Predict the minor and major product DIPEA-diisopropylethylamina or Hunig s base DcJe malc prcducl rnE prcducl Predict products and indicate which one major product 4meducl ShowIne machansm oline lollowing reaclions Clearly](https://cdn.numerade.com/ask_images/a2f1cafde6ec4b419903fdfa7e1a3cab.jpg)
SOLVED: Predict the minor and major product DIPEA-diisopropylethylamina or Hunig s base DcJe malc prcducl rnE prcducl Predict products and indicate which one major product 4meducl ShowIne machansm oline lollowing reaclions Clearly
![DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy](https://l450v.alamy.com/450v/2c5ntm1/dipea-nn-diisopropylethylamine-hunigs-base-molecule-stylized-skeletal-formula-chemical-structure-atoms-are-shown-as-color-coded-circles-hydrogen-hidden-carbon-grey-2c5ntm1.jpg)
DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy
![7087-68-5 | N,N-Diisopropylethylamine | 1,1'-Dimethyltriethylamine; Bis(1-methylethyl)ethylamine; DIEA; DIPEA; Diisopropylethylamine; Ethyl-N,N-diisopropylamine; Ethyldiisopropylamine; Huenig's base; Hunig's base; Hunig's reagent; N,N-Bis(1-methylethyl ... 7087-68-5 | N,N-Diisopropylethylamine | 1,1'-Dimethyltriethylamine; Bis(1-methylethyl)ethylamine; DIEA; DIPEA; Diisopropylethylamine; Ethyl-N,N-diisopropylamine; Ethyldiisopropylamine; Huenig's base; Hunig's base; Hunig's reagent; N,N-Bis(1-methylethyl ...](https://www.trc-canada.com/prod-img/D493340.png)
7087-68-5 | N,N-Diisopropylethylamine | 1,1'-Dimethyltriethylamine; Bis(1-methylethyl)ethylamine; DIEA; DIPEA; Diisopropylethylamine; Ethyl-N,N-diisopropylamine; Ethyldiisopropylamine; Huenig's base; Hunig's base; Hunig's reagent; N,N-Bis(1-methylethyl ...
![DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy](https://c8.alamy.com/zooms/6/92a47d9e82bf42a5be725e509c804409/2c5ntjt.jpg)
DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy
![DIPEA-Promoted Reaction of 2-Nitrochalcones with Elemental Sulfur: An Unusual Approach to 2-Benzoylbenzothiophenes | Organic Letters DIPEA-Promoted Reaction of 2-Nitrochalcones with Elemental Sulfur: An Unusual Approach to 2-Benzoylbenzothiophenes | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b02321/asset/images/large/ol-2017-02321b_0004.jpeg)
DIPEA-Promoted Reaction of 2-Nitrochalcones with Elemental Sulfur: An Unusual Approach to 2-Benzoylbenzothiophenes | Organic Letters
![DIPEA-induced activation of OH − for the synthesis of amides via photocatalysis - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02107B DIPEA-induced activation of OH − for the synthesis of amides via photocatalysis - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02107B](https://pubs.rsc.org/image/article/2022/RA/d2ra02107b/d2ra02107b-f1_hi-res.gif)
DIPEA-induced activation of OH − for the synthesis of amides via photocatalysis - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02107B
![Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N‐ Diisopropylethylamine and 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol - Imada - 2020 - ChemElectroChem - Wiley Online Library Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N‐ Diisopropylethylamine and 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol - Imada - 2020 - ChemElectroChem - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/bc92a293-42f8-4eee-ad78-fc52203605c6/celc202000275-toc-0001-m.jpg)
Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N‐ Diisopropylethylamine and 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol - Imada - 2020 - ChemElectroChem - Wiley Online Library
![Scheme 40. Application of N,N-Diisopropylethylamine (DIPEA) for the... | Download Scientific Diagram Scheme 40. Application of N,N-Diisopropylethylamine (DIPEA) for the... | Download Scientific Diagram](https://www.researchgate.net/publication/331478014/figure/fig2/AS:757545417330689@1557624310427/Scheme-40-Application-of-N-N-Diisopropylethylamine-DIPEA-for-the-synthesis-of.png)