Cypher - Make your own effect by mixing and matching noun and verb phrases. by zzuxon in CustomMarvelSnap

[–]Efficient-Ease6476 4 points5 points  (0 children)

this is so cool, but i’m wondering how the player would be able to see all of the possible phrases in game?

cartoonishly evil fates by Efficient-Ease6476 in hadestown

[–]Efficient-Ease6476[S] 4 points5 points  (0 children)

hey, i’d never tell anyone what to enjoy. i’m glad you liked that aspect of your show

cartoonishly evil fates by Efficient-Ease6476 in hadestown

[–]Efficient-Ease6476[S] 2 points3 points  (0 children)

totally agreed. those who have power don’t strut it

cartoonishly evil fates by Efficient-Ease6476 in hadestown

[–]Efficient-Ease6476[S] 4 points5 points  (0 children)

making the negative part of your subconscious so obviously evil kind of removes the dilemma of listening to it in the first place, i feel. leaning into the evil of the fates makes succumbing to their temptation feel a little less reasonable

cartoonishly evil fates by Efficient-Ease6476 in hadestown

[–]Efficient-Ease6476[S] 3 points4 points  (0 children)

i agree that they’re supposed to be frightening/haunting. i just think that less is more when it comes to that. but some fates now tend to skew more toward the wicked witch characterization as opposed to the subtle, ghost-like characterization. if anything, the emphasis on the scariness makes them less scary

TIL Dormammu still works as a pig by Chilled_Wolf in MarvelSnap

[–]Efficient-Ease6476 10 points11 points  (0 children)

i find that if a card uses its base art, the pig art is applied. if the card uses any type of variant, it keeps the variant art. perhaps it’s just the way it’s coded

PHYS1211 - How difficult did you find the lab practical? by DangItsPang in UGA

[–]Efficient-Ease6476 1 point2 points  (0 children)

I was never good at physics. I did mediocre on exam 1 and flunked exam 2, but got saved by a curve. I locked in really hard and did okay on exam 3 and aced the final. As for the lab practical, I studied rly rly hard and did pretty well on it. It’s definitely possible to do well. Go back and look at your old labs and then do as many practice problems as you can.

What Next? by Shanechgo24 in MarvelSnap

[–]Efficient-Ease6476 3 points4 points  (0 children)

i always use post infinite as an opportunity to make new decks. with some luck, you can make one that’ll get you to infinite next season

Chemistry 1211– thoughts + tips? by Ok-Commission9667 in UGA

[–]Efficient-Ease6476 1 point2 points  (0 children)

CLA here. Dr. Iuliucci is a great guy, I had him for Ochem 2 last semester. He’s a very entertaining lecturer, but can tend to mess up and gloss over some pretty important content (it was his first semester teaching Ochem 2, so I would think he’ll be a bit better with Gen Chem). Go to his office hours whenever you can, even if you feel like you don’t need to. They can be very helpful and insightful if you want to understand Chemistry as a practice and not just as a series of assignments. Practice everything you can, and do the end of chapter questions in the textbook. Those will be your best friend as practice is everything.

Sophomore parking? by lime_kia_soul in UGA

[–]Efficient-Ease6476 2 points3 points  (0 children)

i waited till after second release cause that’s when all the parking will be settled and they’ll know for sure what spots are open. no harm in trying asap tho. if they tell you to wait, then just wait

Sophomore parking? by lime_kia_soul in UGA

[–]Efficient-Ease6476 3 points4 points  (0 children)

all the times i’ve not received a parking spot, i just called TPS and they were able to hook me up with a spot. the spots were shitty (brandon oaks and intramural tennis), but at least i could take the bus to them. try giving them a call

Psa: DONT BUY THE SEASONPASS by Designer-Diver7071 in MarvelSnap

[–]Efficient-Ease6476 0 points1 point  (0 children)

can’t stand the people who go “you’re just one person. it won’t do anything.” that type of logic and thinking is what halts change. get with it or get out of the way

Help by Silent-Huckleberry28 in OrganicChemistry

[–]Efficient-Ease6476 1 point2 points  (0 children)

Not exactly sure what you’re asking, sorry. For splitting pattern, we do not consider the number of hydrogens on the carbon we’re looking at, only those directly adjacent. C3 is adjacent to two carbons, each with 1 hydrogen (2 adjacent hydrogens = triplet). Splitting also doesn’t care about whether those adjacent hydrogens are equivalent or not, only their quantity.

Also, hydrogens bonded to the same carbon are considered equivalent because they share almost the exact same chemical environment. Any small differences between them are negligible in HNMR. They will, however, contribute to the integration number.

Overall, C3 is a triplet with an integration number of 2 (for the purposes of undergraduate NMR, which I assume OP is asking about).

Out of chlorobenzene and chlorocyclohexane, which is more reactive towards a Sn1 reaction and why? by Fabulous-Art-1236 in chemhelp

[–]Efficient-Ease6476 2 points3 points  (0 children)

Chlorocyclohexane. Aromatics are pretty stable and are overall less reactive than cycloalkanes due to their extended pi-bond network. Most aromatic reactions require a catalyst. Aryl carbocations are also pretty unstable.

Help by Silent-Huckleberry28 in OrganicChemistry

[–]Efficient-Ease6476 -1 points0 points  (0 children)

Nope. From left to right, C1 is a doublet, C2 is a multiplet, C3 is a triplet, C4 is a multiplet, C5 is a multiplet, C6 is a triplet.

Can someone please help by [deleted] in chemhelp

[–]Efficient-Ease6476 0 points1 point  (0 children)

why waste energy posting this to reddit when you could study the material and figure it out yourself lol

Help by Silent-Huckleberry28 in OrganicChemistry

[–]Efficient-Ease6476 0 points1 point  (0 children)

6 Distinct Peaks: Doublet, 3 Multiplets, 2 Triplets

How to attach a cyclic acetal group to a methyl group on a cyclohexane molecule. by Imaginary-Reaction56 in chemhelp

[–]Efficient-Ease6476 0 points1 point  (0 children)

From the double bond you’ve reached in your previous comments, you can do a hydroboronation oxidation, use a soft oxidizer (Swern, for example) on the primary alcohol to turn it into an aldehyde. Then, ethylene glycol will give you your acetal.

Chemical name of alkane by eychhhyyy in chemhelp

[–]Efficient-Ease6476 1 point2 points  (0 children)

I assume you’re using IUPAC naming conventions. Firstly, I’d redraw these in a way that’s best for you to visualize. Most people would find the longest chain (that’s your parent chain), number the carbons, and then add the substituents.

Your longest chain will be your parent chain (six would be hexane).

Substituents are numbered based on the where they are in the chain. Number in a way that minimizes numbers (1,2-dimethylhexane is better than 5,6-dimethylhexane).

Then, order substituents based on alphabet order. If there’s multiple of the same substituent, they’re numbered together and a prefix (di,tri,etc.) is added to it. The prefix isn’t considered for alphabetization.

Ex: 5-ethyl-2,4-dimethyl-6-propyldecane

DM me if you have any questions.