![Use Grignard reagents to make a primary, a secondary, and a tertiary alcohol. At least one of the three must involve an epoxide as the electrophile. You do not have to show Use Grignard reagents to make a primary, a secondary, and a tertiary alcohol. At least one of the three must involve an epoxide as the electrophile. You do not have to show](https://homework.study.com/cimages/multimages/16/u21n6730810491790073680.jpg)
Use Grignard reagents to make a primary, a secondary, and a tertiary alcohol. At least one of the three must involve an epoxide as the electrophile. You do not have to show
One-Pot Synthesis of Homoallylic Ketones from the Addition of Vinyl Grignard Reagent to Carboxylic Esters | Organic Letters
![Molecules | Free Full-Text | Regioselectivity in Reactions between Bis(2-benzothiazolyl)ketone and Vinyl Grignard Reagents: C- versus O-alkylation—Part III Molecules | Free Full-Text | Regioselectivity in Reactions between Bis(2-benzothiazolyl)ketone and Vinyl Grignard Reagents: C- versus O-alkylation—Part III](https://www.mdpi.com/molecules/molecules-23-00171/article_deploy/html/images/molecules-23-00171-sch001.png)
Molecules | Free Full-Text | Regioselectivity in Reactions between Bis(2-benzothiazolyl)ketone and Vinyl Grignard Reagents: C- versus O-alkylation—Part III
![Synthesis of the Grignard reagent of (4-vinylphenyl) magnesium bromide. | Download Scientific Diagram Synthesis of the Grignard reagent of (4-vinylphenyl) magnesium bromide. | Download Scientific Diagram](https://www.researchgate.net/publication/263373081/figure/fig1/AS:401897040171009@1472831129934/Synthesis-of-the-Grignard-reagent-of-4-vinylphenyl-magnesium-bromide.png)
Synthesis of the Grignard reagent of (4-vinylphenyl) magnesium bromide. | Download Scientific Diagram
![Titanocene -catalyzed alkylative dimerization of vinyl Grignard reagent using alkyl halides - Chemical Communications (RSC Publishing) DOI:10.1039/B813596G Titanocene -catalyzed alkylative dimerization of vinyl Grignard reagent using alkyl halides - Chemical Communications (RSC Publishing) DOI:10.1039/B813596G](https://pubs.rsc.org/image/article/2008/CC/b813596g/b813596g-s1.gif)
Titanocene -catalyzed alkylative dimerization of vinyl Grignard reagent using alkyl halides - Chemical Communications (RSC Publishing) DOI:10.1039/B813596G
![Grignard coupling-based synthesis of vinyl-substituted hydridopolycarbosilane: effect of starting material and polymerization behavior - RSC Advances (RSC Publishing) DOI:10.1039/D1RA00244A Grignard coupling-based synthesis of vinyl-substituted hydridopolycarbosilane: effect of starting material and polymerization behavior - RSC Advances (RSC Publishing) DOI:10.1039/D1RA00244A](https://pubs.rsc.org/image/article/2021/RA/d1ra00244a/d1ra00244a-f3_hi-res.gif)
Grignard coupling-based synthesis of vinyl-substituted hydridopolycarbosilane: effect of starting material and polymerization behavior - RSC Advances (RSC Publishing) DOI:10.1039/D1RA00244A
![organic chemistry - Rearrangement of Grignard reagent formed from exocycloproyl vinyl bromide - Chemistry Stack Exchange organic chemistry - Rearrangement of Grignard reagent formed from exocycloproyl vinyl bromide - Chemistry Stack Exchange](https://i.stack.imgur.com/FoSjJ.png)
organic chemistry - Rearrangement of Grignard reagent formed from exocycloproyl vinyl bromide - Chemistry Stack Exchange
![Five isomeric alkenes (all positional isomers) A to E , all on catalytic hydrogenation with H2/Pt gives the same optically active alkane F . Only A and B are optically active and Five isomeric alkenes (all positional isomers) A to E , all on catalytic hydrogenation with H2/Pt gives the same optically active alkane F . Only A and B are optically active and](https://dwes9vv9u0550.cloudfront.net/images/9144117/7f044c69-dc6d-4880-8d62-6e611f2036e9.jpg)
Five isomeric alkenes (all positional isomers) A to E , all on catalytic hydrogenation with H2/Pt gives the same optically active alkane F . Only A and B are optically active and
![Vinylmagnesiumbromid, 0.7 M Lösung in THF, AcroSeal , Thermo Scientific Chemicals | Fisher Scientific Vinylmagnesiumbromid, 0.7 M Lösung in THF, AcroSeal , Thermo Scientific Chemicals | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/CCG/Chemical-Structures/chemical-structure-cas-1826-67-1.jpg-650.jpg)
Vinylmagnesiumbromid, 0.7 M Lösung in THF, AcroSeal , Thermo Scientific Chemicals | Fisher Scientific
![Nickel-Catalyzed Cross-Electrophile Vinyl–Vinyl Coupling: An Approach to Structurally Versatile Dienylboronates | CCS Chem Nickel-Catalyzed Cross-Electrophile Vinyl–Vinyl Coupling: An Approach to Structurally Versatile Dienylboronates | CCS Chem](https://www.chinesechemsoc.org/cms/asset/b02a2be4-f271-406b-8956-38d784aedca1/keyimage.jpg)
Nickel-Catalyzed Cross-Electrophile Vinyl–Vinyl Coupling: An Approach to Structurally Versatile Dienylboronates | CCS Chem
![Enantioselective vinylation of aldehydes with the vinyl Grignard reagent catalyzed by magnesium complex of chiral BINOLs - Wang - 2019 - Chirality - Wiley Online Library Enantioselective vinylation of aldehydes with the vinyl Grignard reagent catalyzed by magnesium complex of chiral BINOLs - Wang - 2019 - Chirality - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/05ddfb5d-a7bc-46f6-8b5b-e1370b6494fb/chir23038-fig-0003-m.jpg)
Enantioselective vinylation of aldehydes with the vinyl Grignard reagent catalyzed by magnesium complex of chiral BINOLs - Wang - 2019 - Chirality - Wiley Online Library
![SOLVED: d. (2 pts) If you added vinyl magnesium bromide to your aldehyde and performed the work-up procedure, draw the product you would obtain: e. (4 pts) You desired to make the SOLVED: d. (2 pts) If you added vinyl magnesium bromide to your aldehyde and performed the work-up procedure, draw the product you would obtain: e. (4 pts) You desired to make the](https://cdn.numerade.com/ask_images/d16d3b5552f94cd295c3d17fb14148c7.jpg)
SOLVED: d. (2 pts) If you added vinyl magnesium bromide to your aldehyde and performed the work-up procedure, draw the product you would obtain: e. (4 pts) You desired to make the
![Enantioselective vinylation of aldehydes with the vinyl Grignard reagent catalyzed by magnesium complex of chiral BINOLs - Wang - 2019 - Chirality - Wiley Online Library Enantioselective vinylation of aldehydes with the vinyl Grignard reagent catalyzed by magnesium complex of chiral BINOLs - Wang - 2019 - Chirality - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/3f296ce1-10e4-48cd-8894-786fd4557768/chir23038-fig-0002-m.jpg)