Comments on: Synthesis (4) – Alkene Reaction Map, Including Alkyl Halide Reactions https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/ Sat, 20 Jan 2024 09:21:12 +0000 hourly 1 https://wordpress.org/?v=6.6.2 By: Pramod Rao https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-574060 Tue, 31 Dec 2019 15:36:44 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-574060 Great blog Prof!
The 3rd problem set, 1st reaction. The Hydroboration oxidation. In the answer shouldn’t you show that it is a syn-addition?

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By: Alkene Reaction Cheat Sheets – The Curious Knowledge Wall https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-571613 Tue, 26 Nov 2019 12:34:02 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-571613 […] 150×150 (Found at ‘leah4sci.com/tag/alkyne-reactions’) Size: 791×2463 (Found at ‘https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes&#82…)

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By: James Ashenhurst https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-556295 Thu, 13 Jun 2019 19:29:54 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-556295 In reply to Yo.

The advantage of oxymercuration is that there are no carbocation rearrangements.

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By: James Ashenhurst https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-555174 Mon, 13 May 2019 16:16:21 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-555174 In reply to Ricardo.

Glad you find it useful Ricardo!

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By: Yo https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-518691 Wed, 23 Aug 2017 13:48:18 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-518691 what advantage does the oxymercuration reaction have over the other reaction for formation of alcohols that has the same regioselectivity?

I don’t know.

what are two methods of forming alkyl halides form alkenes that have opposite regioselectivity?
1.HBr, peroxide radical addition
2.HBr

using reactions we’ve learned before, how can the sequence alkane –>Br2. alkyl halide –>use NaOH. alkene —> epoxide .use mCPBA

using reactions we’ve learned before, how can the sequence alkane –> alkyl halide –> alkene –> alkane be accomplished?
1.Br2,HV

2.NaOH
3.H2,Pt,C

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By: Jai https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-488336 Sun, 23 Oct 2016 19:16:24 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-488336 >>At 25th point, Iodohydrin formation, it should be Iodine. Chlorine is written.
>>Can Ag silver catalyst (instead of RO3H) be used to form epoxides from alkenes?
>>Oxidative cleavage of 2-Methlypropene with Hot, Acidic KMnO4 gives Propanone, carbon dioxide and water. The trick (see point no. 31) you mentioned above doesn’t apply here (C-H bonds are not oxidised to C-OH).

Thanks for the great website. It has helped me a lot.

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By: James https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-423840 Mon, 14 Sep 2015 16:57:24 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-423840 In reply to Ethan.

ChemDraw. You probably have access to it for free at your educational institution.

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By: Ethan https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-423235 Fri, 11 Sep 2015 21:38:54 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-423235 What program did you use to draw the molecules and make the concept map? I am trying to keep all the reactions I know straight!!

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By: Ricardo https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-329895 Mon, 24 Nov 2014 18:08:43 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-329895 Thanks a lot for the chart, it beautifully collects all of these reactions in an easy to visualize way. Keep doing what you do!

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By: Rachel https://www.masterorganicchemistry.com/2014/01/21/synthesis-reactions-of-alkenes/#comment-72386 Sat, 01 Mar 2014 21:08:37 +0000 https://www.masterorganicchemistry.com/?p=7919#comment-72386 This is an absolutely great resource as I try to recap and get these back in my head from Org 1 as we start synthesis in Org 2. Do you know of a website or etc. as a good drilling or practice resource? Thanks again for all your posts!!!

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