Yt News today: Youtube daily report Aug 26 2017

hi friends welcome to a mermaid speedpaint video I did the sketch long

time ago in may I sink for a mermaid event but I am coloring it only now and really

feel so tired of this black outlines so for this piece I have used a violet

color and I really liked how it came out by the way it is a waterproof inks from

Koh-i-noor and I did a review video not long time ago so you can check it out if

you want and as always you can find all information about art supplies that I've

used for this painting in the description box below I was trying to

make this mermaid look so tender and I wanted to use a lot of pinks and make a

really dark background with a lot of seaweed and I had a lot of fun with

this piece and I hope you will like my mermaid too and I really want to do more

watercolors would you like to see more watercolors or you wanna marker art?

and for now please enjoy watching see you next video

thank you for watching I hope you liked my mermaid and if you do don't forget to

put thumbs up leave comments and subscribe to my channel to not miss new

video I love all of you bye bye

For more infomation >> Pink Mermaid 🌸 Watercolor + Colored Pencils Painting - Duration: 5:38.

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Ford Focus Wagon 1.5 TDCI 120pk Titanium Edition =RIJKLAAR= Nieuw model / Navigatie / PDC v+a / Tele - Duration: 0:42.

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Getting Guanidine Carbonate and Hydrochloride from No-Lye Hair Relaxants - Duration: 5:18.

Greetings fellow nerds.

I need a source of guanidine for my series on making pyrimethamine.

This is because guanidine is actually a key part of the structure of pyrimethamine as you can see here.

At first i tried making it from urea and sulfamic acid but that didn't turn out too well.

Now other amateurs have been wildly successful so it's probably really easy and i'm just really lazy.

Nonetheless i did find another source of guanidine.

It's actually a component of hair relaxants.

People with stiff curly hair that want to straighten it out use these hair relaxant products.

It's strongly alkaline and softens the hair so it can be combed out.

Once in the desired shape it's neutralized and then holds the new shape.

Most products use sodium hydroxide as a base base but consumers have asked for alternatives so this no-lye version uses guanidine instead as the strong base.

To be sure, check on the ingredients list and somewhere one of the components should be guanidine, usually in the form of guanidine carbonate.

Now this also has plenty of other ingredients like dyes, surfactants, perfumes and other oils.

So we're going to have to run a few purification steps to get our guanidine.

Anyway, let's unbox our hair relaxant.

There is actually a lot of extra products like activators, shampoos and washes but we want just the component that has our guanidine.

And here it is, the liquid activator as it's called.

Doesn't look like much, let's see what we can get out of it.

Pour all of the liquid activator into a beaker.

The guanidine is all dissolved in solution so to precipitate it out we add six times its volume of acetone.

Since the starting volume was 50mL i'm using 300 mL of acetone.

In going with the theme of using stuff from the drug store i'm using a bottle of nail polish remover.

As we add it with stirring the guanidine carbonate precipitates out as it's insoluble in acetone.

Now i'd like to say my selection of six times the volume was some thorough scientific calculation with deep seated theoretical underpinnings.

But in reality i just selected that amount because the bottles of nail polish remover are sold in that size.

You'd be amazed, and probably mortified, at how much top level research is just eyeballed by the researchers.

Anyway, now we simply vacuum filter our guanidine carbonate.

Be sure to wash out the guanidine carbonate with some more acetone to remove as much of the additives as possible.

And that's it, guanidine carbonate.

Now a lot of the additives are in the filtrate but some precipitated out and are stuck to the guanidine carbonate.

So we're going to need to get those out aswell.

Change out the filtering flask since we're going to be collecting our guanidine in it.

Now to the guanidine carbonate on the filter, add hydrochloric acid until it dissolves.

I used about 50mL of 30% concentration although looking back this was probably far too much.

This converts the guanidine carbonate to guanidine hydrochloride which is highly soluble.

It's also known as guanidinium chloride.

The bubbles you're seeing are carbon dioxide.

Today is a very humid day in my lab so the hydrochloric acid is misting up like this.

Anyway once everything is dissolved, turn on the vacuum and filter the solution through.

Now we have our solution of guanidinium chloride.

I wanted to precipitate it back out with more acetone but it turns out it's extremely soluble even in a mixture of acetone water.

Nonetheless the acetone does help us remove more additives because some of them will congeal into some type of slime as seen here.

I'm not exactly certain which additive it is, but whatever it is, i don't want it in my guanidinium chloride.

So we filter it back out again to get our purified solution.

Now we vacuum distill the solution to get dry guanidinium chloride.

My vacuum source is the aspirator pump i showed in a previous video.

I'm using vacuum distillation because it's faster than regular distillation and it's gentler in that you can use lower temperatures.

Also guanidinium hydrochloride is notoriously hygroscopic so simple heating requires very high temperatures to render it dry.

We're going to need it as dry as possible for our synthesis of pyrimethamine.

I set my hotplate to about 130 celsius and also enclosed the boiling flask in a foil shroud to keep the heat in.

After the last drop comes over, let it run for another hour to ensure the guanidinium chloride is as dry as possible.

Then quickly transfer it to an airtight container.

And there it is, guanidinium chloride.

The total mass is 15g.

This is a ludicrously expensive source for this chemical for this amount and i should probably figure out how to make it for cheaper.

But for now I can move on to my pyrimethamine synthesis as this the last precursor.

There is nothing left to do now except make pyrimethamine or fail trying.

Special thank you to all of my supporters on patreon for making these science videos possible

with their donations and their direction.

If you are not currently a patron, but like to support the continued production of science videos like this one,

then check out my patreon page here or in the video description.

I really appreciate any and all support.

For more infomation >> Getting Guanidine Carbonate and Hydrochloride from No-Lye Hair Relaxants - Duration: 5:18.

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React特別篇--霍格華茲學院分配測驗(中文字幕) - Duration: 6:55.

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5 Secrets To Make A Man Madly Fall In Love - Duration: 1:52.

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What does penates mean? - Duration: 0:42.

For more infomation >> What does penates mean? - Duration: 0:42.

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REUPLOAD - Make 2-(p-chlorophenyl)-3-oxopentanenitrile - Step 5 in Pyrimethamine Synthesis - Duration: 9:58.

Warning: Sodium is a dangerous reactive metal.

P-chlorophenyl acetonitrile and dioxane are carcinogenic.

Wear gloves and work outside or in a fume hood.

Methanol is flammable and reactions with sodium are fire hazards.

Fire safety protocols must be in place.

Greetings fellow nerds.

I finally got the next the step of pyrimethamine synthesis to work so in this video we're going to make 2-(p-chlorophenyl)-3-oxopentanenitrile.

This is step 5 of the pyrimethamine synthesis.

First we start with 300mL of methanol dried and distilled from molecular sieves 3A as i've shown in a previous video.

Setup on top a reflux condenser.

Now get 15g of sodium metal.

I showed how to make this in a previous video using magnesium, sodium hydroxide and dioxane.

Links are in the video description.

Cut and roll the sodium into wires like this so we can drop them through the condenser.

Now one by one drop them in with the cooling water turned on.

Don't drop in too much at once or the bubbling will go out of control.

Drop in a piece at a time and let the bubbling get back under control before dropping in more.

What we're doing is reacting sodium with methanol to make sodium methoxide while generating hydrogen gas.

In previous video i showed you can also make sodium methoxide by reacting sodium hydroxide and methanol

and then removing the water with molecular sieves.

That method is much slower than using sodium metal but much safer since it never overheats.

Adding sodium to methanol is dangerous in that it can get so hot that it catches fire.

Considering that methanol and hydrogen gas are both highly flammable this can go very bad very quickly.

Nonetheless, because this is a very fast method and clean method, it's the preferred method in most laboratories.

You also don't get contamination by molecular sieve dust which can be problem for some reactions.

Eventually all the sodium will react and we'll have a solution of sodium methoxide in methanol.

Now reassemble your reflux apparatus into a distillation apparatus and distill off the methanol.

We want relatively solvent free sodium methoxide for the next step.

The reason why we started with excess methanol rather than stoichiometric is because solid sodium methoxide can precipitate out.

This blocks further reaction so it's almost impossible to perfectly react sodium and methanol in a 1:1 ratio.

So we add excess methanol and then remove it by distillation.

Don't discard this distilled methanol.

It's still pure and it's also water free which is useful for upcoming videos where we'll need it again.

Now the final amount of methanol is very hard to boil off so put a shroud around the flask and increase heating to around 250 celsius.

Keep heating until no more methanol distills over.

You can tell when you see the distillate temperature start dropping.

Now turn off the heating, stopper the flask and then let it cool.

We want to minimize the amount of moisture that gets into our sodium methoxide.

While it's cooling we can prepare our reagents.

Get 30g of p-chlorophenyl acetonitrile that we made in a previous video.

Then add 30 mL of ethyl propionate that we also made in a previous video.

All links are in the video description.

Shake it up until everything is dissolved.

Now to the cooled sodium methoxide, add the reagents.

Now add enough dioxane so the total volume is about 300mL.

We made dioxane in a previous video from sulfuric acid and antifreeze and dried it using sodium magnesium oxide aggregate.

Now assemble a reflux condenser onto the flask again and gently heat until it starts refluxing.

What we're doing is using the sodium methoxide to deprotonate the p-chlorophenyl acetonitrile and then react that with ethyl propionate to make 2-(p-chlorophenyl)-3-oxopentanenitrile.

Looking back, i forgot to break up the cake of sodium methoxide first, but eventually with enough stirring it'll break up on its own.

Now as it runs it may foam up.

Adjust heating and stirring to keep foaming under control.

But try and keep it as hot as possible.

Anyway, it's no secret i've been trying to do this reaction for the past 8 months and always failed.

I even used exotic reagents like tetrahydrofuran and potassium t-butoxide.

But i never got it to work.

I was almost ready to give up when i posted my problems here on youtube and a number of you saw right away what was causing my failures.

I was working on a too small a scale.

Even without knowing my scale you knew what the problem was.

It was so much work to make p-chlorophenylacetonitrile i tried to conserve it by working on small 300mg scale.

But for condensation type reactions like this, small scale tends to hurt the process.

Stray water from the air and walls of the glassware can contaminate the reaction and stop it from working.

Scaling up makes the reaction more reliable.

This is one of those times in chemistry where size does matter.

My performance problems for the past 8 months was because i wasn't large enough.

If i had just taken a risk and used everything in one shot this would have worked and i would have been done in january.

Oh well, hindsight is perfect as they say.

I'd like to personally thank Hovsep for emailing me and walking through the problems i was encountering. Thanks.

Anyway, keep heating for 2-3 hours.

Then turn off the heating and let it cool.

Now for aqueous workup and washing.

Get a total of 1 liter of water and fill the reaction flask as much as you can.

Mix it up with a glass stir rod and pour it out.

Wash out the reaction mixture this way.

I didn't just pour it out first because i found the mixture solidifies when cooled.

Adding water first helps make it easier to work with.

Once it's all in the beaker along with 1L of water, stir it for ten minutes or so to thoroughly suspend the chemicals.

Now add in 100mL of 30% or 10 Molar hydrochloric acid and keep stirring for another ten minutes.

Then turn off the stirring and let it settle.

What we're doing is neutralizing the sodium methoxide to sodium chloride and methanol.

The sodium chloride and methanol are very soluble in water and stay in solution while the organic products will separate out.

Most of this is done in a few hours.

But i'm going to let it go overnight.

And here we are the next day.

The organic layer on the bottom should have our product.

Now pour off most of the water and use a separatory funnel to get the rest.

I recommend washing the organic layer again with 100ml or so of water for further purification.

And here is our crude 2-(p-chlorophenyl)-3-oxopentanenitrile.

I sent a sample off for NMR analysis and got back this spectrum.

Over here are the symmetrical aromatic peaks.

This peak over here is the chloroform-d solvent peak since I asked the NMR lab to use chloroform-d for the scan.

This here is that one little proton on the trisubstituted carbon.

It's heavily shifted downfield being connected to such strongly electron withdrawing groups like nitrile, ketone and phenyl.

This spike here is left over dioxane.

It wasn't entirely washed out with the water.

But it's not going to affect our future chemistry so it's not worth putting in additional effort to remove it.

Now for interesting part, this complex multiplet is the protons right beside the ketone and this triplet is the protons at the end.

This complex multiplet is characteristic of our target compound and this is very strong evidence we were successful in making it.

Now this broad peak here is water.

For obvious reasons there is a lot of water contamination.

Overall this spectrum pretty much confirms that we have our desired product.

Our yield is 41g or 99%.

Now i don't think actual synthesis is that good, especially for a garage level synthesis performed using ghetto quality reagents.

The NMR spectrum shows numerous impurities like dioxane and they're probably inflating our numbers.

Literature yields for this procedure range from 50% to 70% so i still think we're doing pretty well.

I'm not going to bother to remove the impurities at this stage since we can remove them later in the next steps on our pyrimethamine synthesis.

So there we have it, after 8 months i finally got to the next step and the hold up was all because i was working on too small a scale.

As you can see the reaction, while very involved, is actually not that hard and if i had done it right the first time i would have been done in january.

Ah well.

Better late than never i guess.

At this point I want to thank you my viewers for believing in me and pushing me forward even though i had essentially given up.

I would have abandoned this if it weren't for you.

Now at this point we should check our map again and see where we are.

We were converting the p-chlorophenyl acetonitrile into 2-(p-chlorophenyl)-3-oxopentanenitrile and have just cleared it.

The last 8 months weren't a total wash though.

We also had to make the solvent dioxane so we can add that to our pathway as an unforeseen detour.

Interestingly enough we also figured how to make sodium metal from domestically available chemicals.

So even if we still totally fail in the upcoming steps we can still say we made a new and useful discovery that justifies our research.

Our next step is the reaction of 2-(p-chlorophenyl)-3-oxopentanenitrile with trimethyl orthoformate.

But before that I'm going to convert the rest of my p-chlorophenyl acetonitrile stock so i have a good amount to use in case I fail more in the future.

And I need to make a video on preparing a guanidine salt.

Hopefully we can finish this project before the end of the year.

Thanks for watching.

Special thank you to all of my supporters on patreon for making these science videos possible

with their donations and their direction.

If you are not currently a patron, but like to support the continued production of science videos like this one,

then check out my patreon page here or in the video description.

I really appreciate any and all support.

For more infomation >> REUPLOAD - Make 2-(p-chlorophenyl)-3-oxopentanenitrile - Step 5 in Pyrimethamine Synthesis - Duration: 9:58.

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Eid Ul Adha 2017 Hajj 2017 Pakistan Hajj Bayan By Maulana Tariq Jameel

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Rin y Len Kagamine Adolescence Sub Español - Duration: 4:42.

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The tale of Elias - 10 opinions of the premiere - Duration: 1:56.

The tale of Elias

10 opinions of the premiere at "Nos Loisirs" cinema

"Fascinating! Work with a very high quality! Congratulations and good continuation."

"First, I became teary-eyed ...

Because it was you the small baby of Franky and Nathalie who was in front of us ...

Then, from the first noises and the first images, I had the goose bump because all which touches the war makes me this effect.

To finish, I realized the scale of the work realized during almost 18 months, but also I told myself that nobody could imagine the difficulty hidden behind this project ..."

We really liked and admired your work, you have a lot of talent and you are a good actor, you make cross a heap of feelings by your look, the tone of your voice, your attitude, in brief we are fans

I found it a little bit short because your short film is by far the best which I saw for a long time. I was conquered by the story and the realization in 3D so I would have wanted that short film is transformed into movie. In brief, I LIKE IT.

The tale of Elias marries quite in sharpness 2 great children lost in a war which exceeds them and a small chap which can help to exorcise their fears. It is a moment of poetry to be shared between children of any ages.

If I had to qualify this short film I would say that it is a remarkable and moving work. It is necessary to have a certain innate professionalism to arrive to create a universe which works. Everything agrees in this short film: the story, the design, the filmed part, the sound, the atmosphere. We are touched by the feelings which gets free of it.

Julien is a promising artist in the world of the cinematographic art.

We regret only a thing in this short film, It is because we want that it becomes a movie

One day who knows

Which work, which result, which wonderfull, just a beginning, But which beginning!

I simply liked, so much the cinema part where I find that you are very good actor, you make cross a lot of sensibility and emotion that on the animation part, very modern as much for the adults as the children.

In a few minutes I found to have spent a just as much pleasant moment that on a feathure film and it tempts us to say .... : the rest

Pressed to see your next projects. In the meantime, we wish you a lot of success and a beautiful long career.

A first short film moving and given rhythm in a graphic universe full of sense. One truth success.

We were lucky and have the honor to present Julien Maingard's movie in private premiere at "Nos Loisirs" cinema at St-Mard. We can say that Julien surprised us by the quality of his work,

he really managed to captivate the spectator with a fascinating scenario, a bright image, a deserving adapted music (see better) students taking out schools of cinemas. And we see many movies.

We count on you to present one day a feathure film in our cinema. It is young people as you and your family who do that we like spreading movies. Good luck for the continuation.

The 1st september on Youtube

For more infomation >> The tale of Elias - 10 opinions of the premiere - Duration: 1:56.

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Sanderson is the band of the week - Aug 25 - Duration: 0:21.

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تغطية معرض جيمز كوم 2017 - تجربتنا للعبة دراجون بول فايترز حصريا - ترجمة الزودياك !! #3 - Duration: 4:19.

For more infomation >> تغطية معرض جيمز كوم 2017 - تجربتنا للعبة دراجون بول فايترز حصريا - ترجمة الزودياك !! #3 - Duration: 4:19.

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Multifandom || That's my girl || TMGC - Duration: 2:15.

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THE GREAT BATTLE OF THE NEW DEMONS! "Killbot vs Digital Descent" (Geometry dash 2.1) - DexTep - Duration: 4:06.

Before starting the video, I'll make a raffle of three geometry dash accounts with 9000 stars! (To participate read the description)

These were the winners of the previous raffle!

New VS! ( ͡° ͜ʖ ͡°)

For more infomation >> THE GREAT BATTLE OF THE NEW DEMONS! "Killbot vs Digital Descent" (Geometry dash 2.1) - DexTep - Duration: 4:06.

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EnaGames Ena - Grave In A Church Walkthrough 2017 - Duration: 6:40.

EnaGames Ena - Grave In A Church

solution: R L R R R R R L L R

For more infomation >> EnaGames Ena - Grave In A Church Walkthrough 2017 - Duration: 6:40.

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How to completely put iPhone 5/5s/6/6s/7/7s in silent mode - Duration: 1:16.

Hello everyone and welcome to my YouTube channel and today in this video we will see how to

put your iPhone in silent mode.

Now in order to put your iPhone in silent mode what you can do is you can just move

this button on the side down.

So, once you put it down you can see see the ringer is silent now.

Now what happens is when someone sends you an SMS or when someone calls you the phone

will not ring.

It will only vibrate.

So, still the phone will vibrate.

If you don't want the phone to vibrate then what you can do is we will go to this "Settings"

here.

We will go to "sounds" here and then you can see vibrate on silent.

Just disable it.

So, what happens now is neither your phone will make sound, nor it will vibrate when

someone calls you or sends you a message.

For more infomation >> How to completely put iPhone 5/5s/6/6s/7/7s in silent mode - Duration: 1:16.

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The Last Enemy - Death

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