Hey Frostpunk 2... What is this?

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#shorts #gaming #frostpunk #funny #livestream #frostpunk2
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You'll find out when you're older Bricky.

Parostem
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How many people even know what the dial up tone is anymore?

nickperri
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Disclaimer this is an understanding of alcohol at A level, the learning qualification immediately before undergraduate study. So take with a grain of salt.
Alcohol- A chemical group defined by its functional group (OH) that is connected, by covalent bond, to a organic chain of 1 or more carbons in length.
Alcohols will have the general structure R-OH.
There are 3 types of alcohols in terms of structure in an organic compound.
Primary-where the OH is bound to a carbon that is bonded to one or less carbons itself, shown as:
(R)-C-OH It is the version that is keast resistant to oxidation and such can form aldehydes and carboxylic acids under distillation and reflux respectively. This is what the simplest forms of alcohol are, including drinking alcohol ethanol, whose molecular formula is CH3CH2OH
Secondary- The OH group is attached to a carbon that is bound to 2 other carbon atoms, and if oxidised will only for a ketone under distillation. Show as (R)2-C-OH
Tertiary alcohols- the carbon attached to OH has 3 carbons attached to it and is resistant to oxidation as to oxidise it would require breaking a carbon to carbon bond.
Shown as (R)3-C-OH.
Note theoretically all alcohols can be combusted which counts as a very extreme form of oxidation, but here these categories have been treated as if reacting with acidified dichromate.

Well what alcohol can you drink?
It is currently acknowledged that it is only safe to drink ethanol (in moderation but that is biology/biochemistry and thus not technically relevant to Bricky's question), methanol is known to cause blindness, and more complex secondary and tertiary alcohols may indeed be used in medicines and other compounds but is in a small dosage and not suitable to my knowledge to drink like one would the ethanol in spirits or other alcoholic drinks.
Alcohols are polar due to the hydroxyl group OH, and as such are water soluble, however, the longer the R group the less soluble the alcohol as the OH group makes up less of the total mass of the compound(it is for example 1 OH per 13 carbons rather than 1 OH per 3 carbons, you may see how the OH has a lesser effect), its boiling points as a group rise the longer the carbon chain it is attached to as the compound gains a greater instantaneous dipole. Understand this is a generalisation, and may be inaccurate if the compound has other groups within it as well, for example a COO-Na where an ionic bond greatly increases its solubility in water.

If i have made any errors please correct me i welcome criticism that is constructive.

NEVER SYNTHESISE ALCOHOL FOR CONSUMPTION WITHOUT APPROPRIATE TRAINING,
INDUSTRIALLY SYNTHESISED ALCOHOL MADE BY HYDRATION REACTIONS ARE NOT SAFE FOR CONSUMPTION DUE TO POTENTIAL PRESENCE OF METHANOL, which as aforementioned may cause BLINDNESS. Always drink responsibly and from fermented sources.
Bibliography using harvard style referencing:
EDIT AT 6/10/2024-corrected spelling mistakes.

Moon-Set-Lane
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Well it has been 10 years for you afterall brickster

ShibaTheWeeb
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Alright Bricky, when a father and a mother love each other very much, they go pray in their bedroom together for a baby they'll love.

rudyyammine
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Procreation: related to Procreate... the software for creating art... (I'll see myself out)

andersonborba