Everything posted by HbWhi5F
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Organic Chem: Dumas method
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Organic Chemistry - Resonance Structure and Electrometric Effect: Need help conceptualizing
-ve O has 8 electrons so it's -2. +O has 8 electrons too and why it's negative.
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Redox Reactions: What takes priority in findng which Element is Oxidized - Add/Remove of H/O, Electron transfer, Electronegative/Positive element ?
@exchemist In (i) What takes priority Electron transfer or Electronegative/Positive element ? I think more electronegative is a good oxidant In (i) Explain addition of Electronegative/Positive element seen as oxidation When the other atoms is more electronegative it is oxidized In (iii) How can Na be oxidized when hydrogen is been added to it ? This part is wierd hydrogen being added is reduced.
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Organic Chemistry Hyperconjugation Resonance: Partial +ve charge on H and neutral C, role of -ve charge on C ?
It seems like a miss-print/render H+ is partially positive but still bonded ? Positive charge needs to be on C for it's empty p-orbital to be stabilized by adjacent C-H bon's sigma bond. What is the role of -ve charge on C ?
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Redox Reactions: What takes priority in findng which Element is Oxidized - Add/Remove of H/O, Electron transfer, Electronegative/Positive element ?
Problem 7.1 In (i) What takes priority Electron transfer or Electronegative/Positive element ? In (i) Explain addition of Electronegative/Positive element seen as oxidation In (iii) How can Na be oxidized when hydrogen is been added to it ?
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Organic Chemistry - Resonance Structure and Electrometric Effect: Need help conceptualizing
Concept If resonance energy is more that means the means resonance structures have varying energies and it should be less stable aka more energy ? So more resonance energy = More Stability ? Problem 8.16 Does the electron movement be of 1 electron and not a pair. C needs 4 more electrons the 2 hooked arrow shows C is getting 1 extra electron. Problem 8.17 Resonance structure needs to have same no. of unpaired electrons. Why charges develop of II Why is O in III +ve Explain “does not contribute as oxygen has positive charge and carbon has negative charge, hence least stable].” Problem 8.18 In II why would O develop +ve charge Explain the answer Electrometric Effect Book says transfer to Pie bond but pie bond atom always looses
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4-Ethyl-2-methylaniline: Why is C2H5 called Ethyl ? and Alternative names ?
Actually 1 wrote "It would be good if some of your countrymen would step in here and tell you that it doesn't hurt to respond to those who have genuinely put themselves out to help you." Many be I am reading it wrong but what is "countrymen" about ?
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Why assume hybridization and not charges on Carbon ?
@exchemist @pinball1970 Sorry if i haven't thanked you for your answer but I do read them, it isn't like I just post question if you feel that way.
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Is Pie bond of Double and Triple Bond CC different ?
@studiot thanks @exchemist
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Organic Covalent Bond Fission: Why it's assumed that +ve ion has a sextet and other 10 electrons ?
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4-Ethyl-2-methylaniline: Why is C2H5 called Ethyl ? and Alternative names ?
@KJW Is there a parent compound priority list? Also thanks for the reply I am being boycotted on the forum. I know I take sometime to reply but somehow that make fellow scholars racist.
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4-Ethyl-2-methylaniline: Why is C2H5 called Ethyl ? and Alternative names ?
@KJW I understand 4-Ethyl-2-methylaniline is the correct name but Is 1-amino-4-Ethyl-2-methybenzene wrong ?
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4-Ethyl-2-methylaniline: Why is C2H5 called Ethyl ? and Alternative names ?
Ethyl is C2H6. Why why C2H5 is called that here ? Aniline means benzenamine (C₆H₅NH₂) but NH2 is at 1. So it can also be written as 1-amino-4-Ethyl-2-methybenzene ?
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Why assume hybridization and not charges on Carbon ?
Example if carbon is bonds to 3 species we assume it's singly bonded with 2 and doubly bonded with 1 and has hybridization of sp2. Why don't we assume sp3 and there is a negative charge on C ? Is it role of hybridization is to form maximum sigma bonds ? All non-hybridized orbitals form pie bonds ?
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How to find no. of bonds between C and O ?
@chenbeier When are triple bonds formed by O ?
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Is Pie bond of Double and Triple Bond CC different ?
@studiot To reiterate the question, the one pie bond in a double bond and 2 pie bonds in a triple bond are they different. I get the hybridization.
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How to find no. of bonds between C and O ?
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Is Pie bond of Double and Triple Bond CC different ?
In (a) Is the Pie bond of Double and Triple Bond CC different that is why written separately in answer
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Need help with derivation of Solubility Product Constant of weak acid. S = {Ksp (H + Ka) / KA}^1/2
Firstly there are what seems to be typos, H has negative charge the latter inverse equation are X instead of H in denominator. Question solubility is for individual ions for salt they is solubility product Ksp ? What is S [f S] and why that equalts to Ksp and S^2 {KS/(Ks + H)} and how is that equal to S = {Ksp (H + Ka) / KA}^1/2 I took me 2+ hours to try and understand this but still don't get it.
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Equilibrium: Why is products assumed to formed in equal amounts ?
@KJW thanks
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Equilibrium: When Pressure is increased x2 is the every species multiplied by 2 ?
- Equilibrium: Is Kc=1/Kc always true ?
- Possible multiple both side by -1 to change sign when RHS has 0 ? a−b+c=-a+b-c
Original question Can one multiply both sides by -1 to flip signs ? Steps - Here RHS is subtracted from both sides, giving us 0 on 1 side x^2- 4.24^2 is combined both sides are multiplied by -1, to flip the signs. that seems like cheating, just flipping signs. If LHS where subtracted from the both sides we would have still got the same result ?- Equilibrium: Is Kc=1/Kc always true ?
- Equilibrium: Why is products assumed to formed in equal amounts ?
- Equilibrium: Is Kc=1/Kc always true ?
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