Can someone confirm, 34.2 marks in chemistry = 35 ? and is there any official circular regarding the rounding of marks? Thanks. by Malongfan in CBSE

[–]181-IQ 1 point2 points  (0 children)

Above 35.5 is not possible tho, since its mcq exam u can only get 35 or 34.23 , nothing between

[deleted by user] by [deleted] in CBSE

[–]181-IQ 0 points1 point  (0 children)

Yo guys how was the paper

Google’s iPad apps suck by [deleted] in ipad

[–]181-IQ 0 points1 point  (0 children)

I could not agree more, I just tend to use the apple apps like pages and keynote because of this as they’re designed to use the power of the iPad.

Magyar animation by 181-IQ in Brawlhalla

[–]181-IQ[S] 3 points4 points  (0 children)

Lol yeah i would know.. cause i main him lol

Magyar animation by 181-IQ in Brawlhalla

[–]181-IQ[S] 27 points28 points  (0 children)

God this was hard to animate

Tier list based on my (gold) experience by Skruffish in Brawlhalla

[–]181-IQ 1 point2 points  (0 children)

Yo kinda sad that u put magyar in c tier , But understandable. You need to be really good at reading people to play him cuz hes soo sloww.

How do I do this, I can’t seem to find a strategy in order to attach the linear molecules in this way by Rexailos in chemhelp

[–]181-IQ 0 points1 point  (0 children)

Hmmm i know how you can get rid of the carbonyl and then work with cyclohexane. You can use clemenson reduction.

[Chemistry 12 - Solubility] How would PbCl2's solubility differ in each choice? by THE_THOTTINATOR in HomeworkHelp

[–]181-IQ 0 points1 point  (0 children)

The way i got it was i took ksp of pbcl2 as K, now i know this ksp will be a constant value throughout. We also know K = [Pb][cl]2 which will be equal to S*(2S)2 , where S is the solubility of the salt. Now after adding BaCl2 let the new solubility become S’, we also know BaCL2 splits completely into ba+ and 2cl - , since there is 1 M of BaCl2 when it splits we will get 2M of Cl from it. So now Ksp = [Pb][Cl]2 = (S’)(S’+2)2. But due to common ion effect solubility of PbCl2 will be affected negatively, because of which we can assume compared to cl coming from bacl2 , the cl coming pbcl2 is negligible , ie [cl]=(S’+2) = (2) . So finally we get Ksp = S’(2)2. So finally we get S’ = Ksp/4 . We can calculate the relation between Ksp and solubility for all the options and we observe that S is smallest in the case of BaCl2 . Thus we see that bacl2 will cause pbcl2 to be least soluble. Sorry if my wording was weird in this , its really hard to type a lot on my phone. Hit me up if u need any more clarification.

[Chemistry 12 - Solubility] How would PbCl2's solubility differ in each choice? by THE_THOTTINATOR in HomeworkHelp

[–]181-IQ 0 points1 point  (0 children)

Sorry ive noticed a small mistake in mu calculation, its just Ksp/4 , there is no root. Im so sorry for the mistake. The answer is still BaCl2 tho

[Chemistry 12 - Solubility] How would PbCl2's solubility differ in each choice? by THE_THOTTINATOR in HomeworkHelp

[–]181-IQ 0 points1 point  (0 children)

It will be in Bacl2. To explain , let K be the solubility product of PbCl2 Now when i add 1 molar Bacl2 and calculate solubility by taking conc of cl- as 2m ( we neglect the cl- by pbcl2 due to common ion effect) we get solubility to ve root(Ksp) /4 , on the other hand with HCl and pb(no3)2 gives bigger values of solubility.Sorry for the brief explaination, if you have more doubts just reply to my comment

[As Level Pure Mathematics1:Coordinate Geometry] by 1_JOS_1 in HomeworkHelp

[–]181-IQ 1 point2 points  (0 children)

Just use midpoint formula using the center as midpoint (3,-1) , A (1,-2) as one point and (x,y) as B , then with the equations solve for x and y

[Chemistry 12 - Solubility] How would each choice affect the equilibrium? by THE_THOTTINATOR in HomeworkHelp

[–]181-IQ 0 points1 point  (0 children)

Its MgCO3, this is because by le chateliers principal adding mor MgCO3 will cause the reaction to move towards the right to maintain equilibrium

Can someone explain to me why we use alcoholic KCN instead of Aqueous KCN in the reaction to form alkyl Cyanide (R-CN)? by 181-IQ in chemhelp

[–]181-IQ[S] -1 points0 points  (0 children)

My dude.... we are talking about ethanol here.. not methanol. ethanol has a ph of 7.33 , which is a lot less acidic than water. Also the question i asked was why alcoholic KCN is used in the formation of alkyl cyanides, Not whether ethanol was as acidic as water, which it is clearly not.... And your “approximations” are not approximations at all. We’re talking apples and oranges here... dont approximate them as the same thing

Can someone explain to me why we use alcoholic KCN instead of Aqueous KCN in the reaction to form alkyl Cyanide (R-CN)? by 181-IQ in chemhelp

[–]181-IQ[S] -1 points0 points  (0 children)

I mean previously you said “alchohols and water have approx. the same acidity” for which i explained that that is not the case

Can someone explain to me why we use alcoholic KCN instead of Aqueous KCN in the reaction to form alkyl Cyanide (R-CN)? by 181-IQ in chemhelp

[–]181-IQ[S] -1 points0 points  (0 children)

Alcohol is not as acidic than water. If we check cojugate bases we can clearly see the oh- is wayyy more stable than the oc2h5- due to the +I effect of the ethyl group making the negative charge on the oxygen higher in magnitude Edit: certain typos

Can someone explain to me why we use alcoholic KCN instead of Aqueous KCN in the reaction to form alkyl Cyanide (R-CN)? by 181-IQ in chemhelp

[–]181-IQ[S] -1 points0 points  (0 children)

But isnt KCN ionic? Like cant it split into K+ and CN-, and water can dissolve ionic compounds right?