In this video we make tertiary alcohols using the (in)famous Grignard reaction.
Briefly, an alkyl halide is reacted with magnesium metal to form an organometallic alkyl magnesium halide. This is the grignard reagent. This reagent is then reacted with a carbonyl containing compound suck as a ketone, an ester or an organic carbonate to form a tertiary alcohol. The mixture is then reacted with water and titrated with acid to dissolve the magnesium hydroxides formed. Finally, the alcohol is purified by a series of liquid extractions and distillations.
Related videos:
Purifying and drying diethyl ether for use in grignard reactions: https://www.youtube.com/watch?v=EEXqjJd0Bak
Making alkyl halides: https://www.youtube.com/watch?v=Ydn1D4FSqkc
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https://www.youtube.com/watch?v=EFQWD7-DCPI
In this video we make a chemiluminescent reaction that is activated by a vapor.
The reaction is very easy to perform: Mix 3mL of dimethyl phthalate, 3mg of fluorescent dye such as rubrene, and 3mL of hydrogen peroxide (30%) and shake. Let the mixture separate and apply the bottom dimethyl phthalate to a surface. Then pass oxalyl chloride vapors over the surface.
The oxalyl chloride vapor will react with the chemicals to produce a strong chemiluminescent glow that will last for a few seconds.
Related videos:
Make glow sticks: https://www.youtube.com/watch?v=tItOOpyJP5k
Ghost metal: https://www.youtube.com/watch?v=VDMgrgSVjd8
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https://www.youtube.com/watch?v=im_2OIs_mns
A full two liters of glow fluid, about as much as you would find in 100 medium sized glow sticks.
Imagine going to a rave and glowsticking with a couple of these!
Not the world's biggest single glow stick, but still awesome.
We made this using all the same chemicals in our previous glow stick making video just scaled up by a factor of 100.
The link is here: http://www.youtube.com/watch?v=kH19EIf5GtE
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https://www.youtube.com/watch?v=mUCdGMeTveM
So i've been trying to make lithium in a similar way to making sodium as shown in previous videos. But lithium synthesis appears to be very slow. Fortunately, this proves that all our previous samples of sodium that was made using lithium is probably very pure since lithium cannot be made under the same conditions.
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https://www.youtube.com/watch?v=crom-TLcCQ4
In these lab notes we attempt terpin hydrate, urushibara nickel and explore sodium production with super-stoichiometric sodium hydroxide.
Related Videos:
"Hydrogenation: transform liquid oil into solid fat" by applied science: https://youtu.be/oqdDWA9-DSY
"Making Margarine: Edible Chem" by Nilered: https://youtu.be/drIm8_1CvjQ
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https://www.youtube.com/watch?v=Jv-tJMg-U4c
Most people break hearts with words. Nerds break hearts with Liquid Nitrogen!
Disclaimer: This is actually a pig's heart that was obtained from a pig that was already being processed into food products. No humans were harmed, or unlawful suffering to animals was caused outside of established food industry practices.
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https://www.youtube.com/watch?v=zLWEemhtdbE
In this video, we make isopropyl nitrite without using sodium nitrite.
Typically, amateur chemists use sodium nitrite, hydrochloric acid, and isopropyl alcohol for this process, but sodium nitrite is becoming harder to obtain. This sodium nitrite-free pathway goes through nitrosylsulfuric acid which can be made using more easily obtained fuming nitric acid and sulfur dioxide.
To make fuming nitric acid from you can use this video: https://youtu.be/88gbfCnrV8o
How to make sulfur dioxide: https://youtu.be/2AFKlLSwUZ4
To begin, we dry 400mL of 99% isopropyl alcohol using molecular sieves 3A (that itself was previously dried at 200 Celsius). In a separate flask, we mix 63g of fuming nitric acid with 150mL of glacial acetic acid, keeping the mixture cool in an ice bath.
To make glacial acetic acid, i refer you to Nile Red: https://www.youtube.com/watch?v=8iG_qnkF08Y
or Amateur chemistry:
https://www.youtube.com/watch?v=FOb4R5_LK-I
Meanwhile, a sulfur dioxide is injected from a sulfur dioxide generator into our nitric acid mixture forming nitrosylsulfuric acid.
After the reaction, the nitrosylsulfuric acid precipitates out. It's filtered and i got a Yield of 117g or 91%. Due to its instability, it must be used promptly. It's slowly combined with chilled isopropanol, creating isopropyl nitrite. Careful addition and temperature control are crucial to prevent decomposition.
After the reaction, we add ice and make up the volume to 1L to separate the isopropyl nitrite. A separatory funnel is used to recover the lighter organic phase of isopropyl nitrite. The final yield is 56g or about 63% based on nitric acid, with an adjusted yield of 69% based on nitrosylsulfuric acid quantity.
While this method may not match the ease of sodium nitrite-based processes, it serves as a valuable alternative for those facing sodium nitrite availability challenges.
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https://www.youtube.com/watch?v=aT1Bylf1_00
In this video i replace the triacs in a broken hot plate stirrer.
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This video was generously sponsored by:
Robert Boll
Kevin S
Only HR
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https://www.youtube.com/watch?v=a3RWe-EZ9UQ
How to make Manganese Dioxide Electrodes that can be used for chlorate cells or HHO cells and a few other electrochemical processes requiring inert anodes in oxidizing solutions.
Make the electrode is fairly simple. First a titanium strip is sanded to give a clean surface and then etched with hydrochloric acid to activate it. Cobalt nitrate solution is applied in a thin layer and then heated to 300 Celsius to decompose (pyrolyze) the cobalt nitrate into cobalt oxide. the loosely adhering cobalt oxide is washed off and then new layers of cobalt oxide are applied. Usually between 3 to 10 layers.
Then manganese nitrate is applied and the process repeated to make manganese dioxide. Another 10 to 50 layers may be applied.
Optionally, a further layer of manganese nitrate by electrolysis may be applied by using the electrode as an anode in a solution of 90 grams manganese sulfate, 500mL water and 12mL concentrated sulfuric acid. Copper or titanium is used as the cathode and a current density of about 10ma per square centimeter is used. A short run time of a few minutes or so puts a thin layer of manganese dioxide on the surface that seems to reduce permanganate production, but does not eliminate it.
In the future i'll be working on a lead dioxide electrode.
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https://www.youtube.com/watch?v=BjKYiu8eKa8