![SOLVED: Pictured below are some nitrogen-containing molecules Ifthe molecule has more than one nitrogen tom, identify the most basic lone pair Rank the molecules in order from strongest base to weakest; and SOLVED: Pictured below are some nitrogen-containing molecules Ifthe molecule has more than one nitrogen tom, identify the most basic lone pair Rank the molecules in order from strongest base to weakest; and](https://cdn.numerade.com/ask_images/7719de3e53a94147a67ee5cc3d848c1b.jpg)
SOLVED: Pictured below are some nitrogen-containing molecules Ifthe molecule has more than one nitrogen tom, identify the most basic lone pair Rank the molecules in order from strongest base to weakest; and
![Base-catalyzed C-alkylation of potassium enolates with styrenes via a metal–ene reaction: a mechanistic study - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02495F Base-catalyzed C-alkylation of potassium enolates with styrenes via a metal–ene reaction: a mechanistic study - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02495F](https://pubs.rsc.org/image/article/2020/OB/c9ob02495f/c9ob02495f-f1_hi-res.gif)
Base-catalyzed C-alkylation of potassium enolates with styrenes via a metal–ene reaction: a mechanistic study - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02495F
![SOLVED: Provide the reaction conditions L0 form the major products as shown below and explain why NaNHz NH; 20 degrees EtBr 1) KHMDS, -78, THF 2) EtBr This is the thermodynamic product SOLVED: Provide the reaction conditions L0 form the major products as shown below and explain why NaNHz NH; 20 degrees EtBr 1) KHMDS, -78, THF 2) EtBr This is the thermodynamic product](https://cdn.numerade.com/ask_images/bf1483f72a5640c787feb45baeb94744.jpg)
SOLVED: Provide the reaction conditions L0 form the major products as shown below and explain why NaNHz NH; 20 degrees EtBr 1) KHMDS, -78, THF 2) EtBr This is the thermodynamic product
![Potassium Base‐Catalyzed Michael Additions of Allylic Alcohols to α,β‐Unsaturated Amides: Scope and Mechanistic Insights - Sai - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library Potassium Base‐Catalyzed Michael Additions of Allylic Alcohols to α,β‐Unsaturated Amides: Scope and Mechanistic Insights - Sai - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d05aa9bb-c8cc-4331-8ce4-0a6dd6b0b7b5/adsc202100272-fig-5001-m.jpg)
Potassium Base‐Catalyzed Michael Additions of Allylic Alcohols to α,β‐Unsaturated Amides: Scope and Mechanistic Insights - Sai - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library
Synthesis of π-Extended Fluoranthenes via a KHMDS-Promoted Anionic-Radical Reaction Cascade | Organic Letters
![Dimeric Potassium Amide-Catalyzed α-Alkylation of Benzyl Sulfides and 1,3-Dithianes | Organic Letters Dimeric Potassium Amide-Catalyzed α-Alkylation of Benzyl Sulfides and 1,3-Dithianes | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.9b01994/asset/images/medium/ol-2019-01994z_0008.gif)
Dimeric Potassium Amide-Catalyzed α-Alkylation of Benzyl Sulfides and 1,3-Dithianes | Organic Letters
![Chemistry, Trimethylsilyl, Potassium, Potassium Amide, Chemical Compound, Lithium Diisopropylamide, Nonnucleophilic Base, Organic Chemistry, Trimethylsilyl, Potassium, Potassium Amide png | PNGWing Chemistry, Trimethylsilyl, Potassium, Potassium Amide, Chemical Compound, Lithium Diisopropylamide, Nonnucleophilic Base, Organic Chemistry, Trimethylsilyl, Potassium, Potassium Amide png | PNGWing](https://w1.pngwing.com/pngs/603/801/png-transparent-chemistry-trimethylsilyl-potassium-potassium-amide-chemical-compound-lithium-diisopropylamide-nonnucleophilic-base-organic-chemistry.png)
Chemistry, Trimethylsilyl, Potassium, Potassium Amide, Chemical Compound, Lithium Diisopropylamide, Nonnucleophilic Base, Organic Chemistry, Trimethylsilyl, Potassium, Potassium Amide png | PNGWing
![Potassium Base‐Catalyzed Michael Additions of Allylic Alcohols to α,β‐Unsaturated Amides: Scope and Mechanistic Insights - Sai - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library Potassium Base‐Catalyzed Michael Additions of Allylic Alcohols to α,β‐Unsaturated Amides: Scope and Mechanistic Insights - Sai - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/326f8ef1-d178-4e4f-a6b5-1b4bfe5a0fda/adsc202100272-toc-0001-m.jpg)
Potassium Base‐Catalyzed Michael Additions of Allylic Alcohols to α,β‐Unsaturated Amides: Scope and Mechanistic Insights - Sai - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library
![Exploring the solid state and solution structural chemistry of the utility amide potassium hexamethyldisilazide (KHMDS) - Dalton Transactions (RSC Publishing) DOI:10.1039/C7DT01118K Exploring the solid state and solution structural chemistry of the utility amide potassium hexamethyldisilazide (KHMDS) - Dalton Transactions (RSC Publishing) DOI:10.1039/C7DT01118K](https://pubs.rsc.org/image/article/2017/DT/c7dt01118k/c7dt01118k-s2_hi-res.gif)
Exploring the solid state and solution structural chemistry of the utility amide potassium hexamethyldisilazide (KHMDS) - Dalton Transactions (RSC Publishing) DOI:10.1039/C7DT01118K
![KHMDS/Triglyme Cryptate as an Alternative to Phosphazene Base in Stereodivergent Pentafluoroethylation of N-Sulfinylimines Using HFC-125 | The Journal of Organic Chemistry KHMDS/Triglyme Cryptate as an Alternative to Phosphazene Base in Stereodivergent Pentafluoroethylation of N-Sulfinylimines Using HFC-125 | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.2c01821/asset/images/medium/jo2c01821_0014.gif)
KHMDS/Triglyme Cryptate as an Alternative to Phosphazene Base in Stereodivergent Pentafluoroethylation of N-Sulfinylimines Using HFC-125 | The Journal of Organic Chemistry
![Exploring the solid state and solution structural chemistry of the utility amide potassium hexamethyldisilazide (KHMDS) - Dalton Transactions (RSC Publishing) DOI:10.1039/C7DT01118K Exploring the solid state and solution structural chemistry of the utility amide potassium hexamethyldisilazide (KHMDS) - Dalton Transactions (RSC Publishing) DOI:10.1039/C7DT01118K](https://pubs.rsc.org/image/article/2017/DT/c7dt01118k/c7dt01118k-s1_hi-res.gif)
Exploring the solid state and solution structural chemistry of the utility amide potassium hexamethyldisilazide (KHMDS) - Dalton Transactions (RSC Publishing) DOI:10.1039/C7DT01118K
![Synthesis of π-Extended Fluoranthenes via a KHMDS-Promoted Anionic-Radical Reaction Cascade | Organic Letters Synthesis of π-Extended Fluoranthenes via a KHMDS-Promoted Anionic-Radical Reaction Cascade | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b01538/asset/images/large/ol-2017-01538a_0009.jpeg)
Synthesis of π-Extended Fluoranthenes via a KHMDS-Promoted Anionic-Radical Reaction Cascade | Organic Letters
![Potassium Amide‐Catalyzed Benzylic C−H Bond Addition of Alkylpyridines to Styrenes - Zhai - 2018 - Angewandte Chemie International Edition - Wiley Online Library Potassium Amide‐Catalyzed Benzylic C−H Bond Addition of Alkylpyridines to Styrenes - Zhai - 2018 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/008ef04e-fa41-455a-9644-045ad7fdf91d/anie201710128-fig-5001-m.jpg)
Potassium Amide‐Catalyzed Benzylic C−H Bond Addition of Alkylpyridines to Styrenes - Zhai - 2018 - Angewandte Chemie International Edition - Wiley Online Library
![Synthesis of π-Extended Fluoranthenes via a KHMDS-Promoted Anionic-Radical Reaction Cascade | Organic Letters Synthesis of π-Extended Fluoranthenes via a KHMDS-Promoted Anionic-Radical Reaction Cascade | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b01538/asset/images/medium/ol-2017-01538a_0005.gif)