Draw the NMR Spectrum of ethanol

[@aa07011]

The OH signal is all the way to the right when it's very concentrated with alcohol. The spectrum you showed is for 10% alcohol and 90% solvent. The more diluted, the more the OH signal shifts upfield to the left.

[@MunsKi]

so we are sending radiowaves to a solution bec we cannot do it in a single molecule.. thanks for clarifying

[@tsshmattb]

thanks for the explanation, I was having alkynes of trouble with NMR interpretation.

[@ralphchen5660]

Same here. I am not alkene on doing these darn NMR analyses in my ochem labs.

[@samh6479]

Same! After this video, we alkane do H NMR analysis.

[@1965dsk]

The spectrum explained was for impure ethanol.I also request you to explain the NMR of PURE SAMPLE OF ETHANOL .

[@anamarbab4644]

Can u help me plz

[@flow4458]

@@anamarbab4644 You gotta say with what, honey.

[@jonathanlalrintluanga4737]

I have exam today on this subject. I love you man... 😘😘😘

[@rekhachoudhary5666]

Sir you explained well....

[@devinlewis5116]

Is it possible SDBS could be incorrect? Literally every other H-NMR spectrum I look up for ethanol has the O-H hydrogen at just under 5 ppm.

[@spotsies]

Note that the distance the peaks appear varies based on the strength of the applied magnetic field, that's my guess why. Using a magnetic field of about 500MHz, the hidroxyl H appears between 5.5 and 5.0 ppm, as opposed the spectrum showed by him was made using abour 89.56MHz.

[@devinlewis5116]

I asked my O Chem professor and he said that both spectra are correct, it is actually the difference between the solvents used. Deuterated chloroform will give the spectrum that SDBS provides, and d-6 DMSO gives the O-H hydrogen around 5 ppm.

[@saikrishnanep2591]

like my friend teaches me, and not another big professor. cool man!

[@elielromero]

There are some effects like the presence of solvents.

[@anjanagopinadh]

Why OH peak is not observed at far position from TMS? Is it more deshielding proton ryt???

[@aroojshahid5658]

why did you applied n+1 rule for the peak splitting?

[@strongbodystrongmiind]

Arooj Shahid tells you the amount of splitting

[@strongbodystrongmiind]

*neighboring hydrogens

[@Neobiology]

How many proton signals do you expect in the PMR spectra of c2h5oh

[@kumar_aashish9237]

What is the spectrum of ch3och3 (dimethyle ether)

[@joelaryea8988]

Please the H on the O shows splitting with the adjacent H so I'm confused 😕 . It shows a triplet

[@ngstudentsvlog113]

Thank you bro

[@therealshedrack]

thanks for the explanation

[@nickthetechy9397]

Good

[@anubhab1525]

Thanks a lot!

[@Lacrossefreak3696]

Thanks for the help!

[@trivenibandi5984]

Thanks sir. It helped me.

[@Medi-Nor]

I used to watch ur videos for chem 1 and 2 I got A's in both classes, now I'm taking orgo I'm struggling.

[@sabirkhannawaz2044]

thanks

[@Medi-Nor]

U the best

[@madhvisaini74]

Thanks for your explanation #galbeautyattitude

[@ryandward]

Your terminology is off. Split twice means 1->2->4. Split three times 1->2->4->8

[@kokilakoki6285]

Tamil ah explain pannunga

[@nausheenquraishee1446]

Pls explain in hindi

[@yizzlephysiq1250]

lern englesh

[@tabithatcheau1571]

In general, why is H bonded to O so downfield?

[@GoodFeelingsOnly]

Oxygen is a very electronegative atom, so it causes a deshielding effect on the H bonded to it (meaning it pulls all the electrons closer to him).