Skip to main content

All Questions

Tagged with
-1 votes
1 answer
669 views

Why does a carbon double bond "break readily" but this is not so for other elements (nitrogen double and triple bonds are stronger)? [duplicate]

A level chemistry student here, fairly basic question. We always learnt (from GCSE bond enthalpies) that "Bigger bonds are stronger", so to speak; my teacher often quoted $\ce{N#N}$ as very ...
FShrike's user avatar
  • 223
1 vote
1 answer
1k views

Bond Polarity vs bond length's effect on reactivity of haloalkanes

My textbook says: Carbon acquires partial positive charge whereas halogen acquires partial negative charge. Halogen becomes nucleophilic in character, which can be replaced by another nucleophile on ...
Shozab Lilani's user avatar
4 votes
0 answers
771 views

Reactivity order among Interhalogens

I was reading about Interhalogens in JD Lee and in the book it is stated that (without any reasoning) the reactivity order for few of the interhalogens is :- $\ce{ClF_3 > BrF_5 > IF_7 > ClF &...
Rishi's user avatar
  • 477
0 votes
1 answer
48 views

Alternative explanation of ethene's pi bond [closed]

This tutorial about ethene's bonds has the following paragraph that I hope someone can paraphrase in a better way: The pi bond dominates the chemistry of ethene. It is very vulnerable to attack - a ...
Jodes's user avatar
  • 461
-2 votes
2 answers
191 views

How do you know what elements will bond in a reaction? [closed]

I know all about the types of reactions, synthesis, decomp. etc., but when a bond is broken, how do you know that the free element will bond to another molecule? Is it because that element has a ...
Pasta Man's user avatar
0 votes
1 answer
158 views

Reason behind more Reactivity of Unsaturated Hydrocarbons [closed]

My textbook says that unsaturated hydrocarbons are more reactive than saturated ones. But double and triple bonds are stronger than single bonds. What is the explanation for this?
Shub's user avatar
  • 408
0 votes
0 answers
16 views

What is the order of acidity for hydrogens in primary, secondary and tertiary alkanes, alkenes, and cycloalkanes [duplicate]

The bond dissociation energies of C-H bonds in alkanes, alkenes and aromatic compounds decrease in the following order: primary > secondary > tertiary > allylic > benzylic. The weaker the bond, the ...
Patrick Tchakounte's user avatar
1 vote
0 answers
69 views

Do amides oxidize to double-bonds?

Do amides from primary or secondary amines ever oxidize to a double-bond on the nitrogen? For example, like from an $\mathrm{R \bbox[yellow]{\color{red}{-}}(NH)-(C=O)-R'}$ to an $\mathrm{ R \bbox[...
ManRow's user avatar
  • 1,556
0 votes
1 answer
548 views

Decomposing chemical compounds - Ease of Decomposition [closed]

Someone asked me a question, that which of the following can be decomposed chemically: Ammonia Iron Neon Hydrogen Fluorine My Analysis: At first attempt I answered Ammonia but changed it to 'I can'...
Shivanshu Gupta's user avatar
4 votes
1 answer
190 views

Nucleic Acids Bonds

In a paper I am reading regarding instability and decay of DNA, the author says: "The chemical price paid for the greatly increased resistance of the nucleic acid phosphodiester bond (gained by ...
Johnathan's user avatar
  • 325
14 votes
2 answers
18k views

Why does N₂ react with O₂ to Form NO at high temperatures?

This also raises questions that I have about the Haber Process which produces ammonia ($\ce{NH3}$) from molecular nitrogen ($\ce{N2}$) and hydrogen ($\ce{H2}$). I have heard multiple times that bond ...
Nick's user avatar
  • 442