Questions tagged [reactivity]

Applied to a chemical species, the term expresses a kinetic property in reference to another species. The tag should be applied to questions seeking answers with respect to the reactivity (or unreactivity) of a certain chemical compound, species, molecular entity and/or functional groups. It must not be applied to questions about the stability of certain chemical species.

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12
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271 views

Aza-enolates: why no reaction at N

My understanding is that aza-enolates have an advantage over enamines in enolate-type alkylations because the reaction at N is less likely. As a result, unactivated electrophiles can be used (i.e. ...
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224 views

Solve this chemical or biological mystery

I hope this is the best place to pose this unique question. Please forgive me if it's not. I went into a closet to get a prescription medication that was filled about a year ago. The label on the ...
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1answer
2k views

Bonding of Lithium and Argon

I saw a meme that was joking around about Lithium and Argon bonding (see pic below). It got me wondering: Can Lithium and Argon bond in any circumstance?
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SN1 reactivity order for chloromethyl methyl ether and trityl chloride

Compare the reactivity order towards SN1 reaction for: (2-chloropropan-2-yl)cyclopropane $\ce{CH3OCH2Cl}$ $\ce{Ph3CCl}$ Owing to the exceptional stability of cyclopropyl ethyl ...
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2k views

How to compare the oxidizing power of perhalate ions

In my book the oxidizing power in descending order of the following is given as: $\ce{BrO4-} > \ce{IO4-} > \ce{ClO4-}$ My doubt is regarding their order of oxidizing tendency. I thought that ...
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40 views

Orbital Interaction for electrophile and nucleophile

Clearly the above diagrams depict the interaction between empty orbital of electrophile with filled orbital of nucleophile. We may assume that the HOMO of nucleophile being more electronegative will ...
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76 views

Reactivity of carbon-centered radical

I've read this site for a long time but I had never asked a question, so this is my first time :). So, i'm currently working on a computational chemistry project on radical cyclization reactions and ...
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93 views

Advanced Quantum Chemistry Reference for Reactivity Phenomena

I'm currently in organic synthesis seeking to develop quantitative "physical" (that of a physicist), rather than "chemical", intuition for areas where traditional VSEPR/ MO models cannot fully ...
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43 views

Reactivity order of DIBAL-H and diborane with esters and acids

I have been taught in class that DIBAL-H is more reactive towards esters than carboxylic acids while opposite is true for diborane. Also DIBAL-H mentioned is taken under low temperatures (−78 °C). I ...
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96 views

Why doesn't 1-cyclopropylethyne give a positive reaction in the bromine-water unsaturation test?

1-cyclopropylethyne has a triple bond: Hence it seems like it should yield a positive unsaturation test with bromine water. But, my book states that the opposite is true. I guess this may be due to ...
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43 views

Competition between aromatic sulphonation and nitration

Say you take a substituted benzene* and react it with oleum and nitric acid. Would it result in a nitrated ring, a sulphonated ring, or some sort of a combination? Thinking about it in terms of the ...
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84 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 &...
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1answer
121 views

p-Nitroaniline reaction with sulfuric acid

An alternative version of the well-known demonstration carbon snake (the dehydration reaction of sugar by concentrated sulfuric acid forming a column of graphite) consists in mixing paranitroaniline ...
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137 views

Silver Tarnish and Reactivity Series

I read that silver in the presence of hydrogen sulfide corrodes to form silver sulfide and hydrogen. $$\ce{Ag + H2S -> AgS + H2}$$ But in the reactivity series silver is placed much below hydrogen. ...
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38 views

Metalation of thiophene

So lately I've been studying the concerted metalation-deprotonation of thiophene and I came to the conclusion that the alpha positions of thiophene are the most reactive, which is why one of those ...
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342 views

Why are “diene” structures in the C-ring of anthocyanins singled out for their singlet-oxygen quenching ability?

Anthocyanins are a class of water-soluble vacuolar pigments. They are sensitive to pH, and can undergo a series of structural changes according to a pH-dependent equilibrium as illustrated in Figure 1....
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822 views

Why is the silver nitrate chemical test more favorable than that of sodium iodide?

Two tests to determine the presence of alkyl chlorides are the silver nitrate in 1% ethanol and sodium iodide in 15% acetone tests. These two tests both produce a precipitate when added to chloride ...
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1k views

Is benzyl chloride or allyl chloride more reactive?

What compound is more reactive, benzyl chloride [(chloromethyl)benzene] or allyl chloride (3-chloroprop-1-ene)? I know that both have a higher reactivity than alkyl and aryl chlorides.
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Constructing a reactivity series, magnesium more reactive than sodium?

I reacted about $0.25 \,\mathrm{g}$ of magnesium, sodium and lithium in $20 \,\mathrm{ml}$ of $2 \,\mathrm{M} \,\ce{HCl}$ at room temperature. This was all done in a $100 \,\mathrm{mL}$ beaker. I ...
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146 views

Could any constituent of normal human urine produce a false positive in a Kastle-Meyer test for presence of blood?

From my understanding, one forensic test for the presence of traces of blood at a crime scene is (or was) the Kastle-Meyer test. Doing some research, I understand that in the test, hemoglobin reacts ...
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85 views

Grignard reaction - exchange of groups

Why is this reaction successful: Why doesn't metal-halide exchange occur easily to get Ar-MgCl and R-Br?
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1answer
741 views

Reactivity of different alcohols with NaNH2 and CH3I

Identify the final product (B) in the following reaction: I'm not sure how $\ce{NaNH2}$ and $\ce{CH3I}$ will react with the different types of alcohol present here. According to my solution,ether was ...
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101 views

Regarding stability and reactivity of m-xylene

I came across the following two details about m-xylene: m-Xylene is thermodynamically most stable compound among o-xylene, m-xylene, and p-xylene. m-Xylene is most reactive towards nitration and ...
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48 views

What does Molecular Orbital Theory allow you to predict?

Molecular Orbital theory reveals the outcome when two atomic orbitals overlap. Almost all of the time we draw a Y axis with the notation of energy that can be described using electron volt units (eV). ...
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73 views

NaOH vs Polypropylene

This source lists polypropylene as suitable for use with NaOH. However, this paper seems to demonstrate that NaOH slowly degrades polypropylene (even at fairly moderate temperatures). Does anyone ...
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282 views

Why do the induction effects of fluorobenzene decrease electrophilic addition reactivity, conjugation effects increase selectivity?

Fluorobenzene shows signs of both the electron withdrawing and electron donating groups on benzene. Electrophilic substitution to the ring is less reactive because the fluorine is very electronegative ...
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229 views

What is the most likely reaction between minocycline and tramadol in physiological conditions?

Minocyline (left) and Tramadol (right) are two commonly prescribed medications containing typical organic functional groups. What would an expert chemist surmise as the first or most-likely reaction ...
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527 views

Why are thioethers not better leaving groups than ethers?

Why are thioethers ($\ce{RSR}$) not better leaving groups than ethers ($\ce{ROR}$)? I learnt that better bases are poorer leaving groups. Here, clearly the poorer base is thioether, as the lone pair ...
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207 views

Can activated charcoal retain adsorbtion properties even when submerged in liquids?

This is following a question on Skeptics Stackexchange, where apparently medical science claims that activated charcoal can adsorb poison when ingested. One of the members posted a related question on ...
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2k views

Naphthalene v/s Anthracene reactivity

Both have similar resonance energy per ring, even Naphthalene has a little higher Resonance energy (127.5 KJ per mol per ring v/s 127 KJ per mol per ring ) Can we prove , why there is a small ...
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0answers
383 views

Ketal formation of ethyl acetoacetate

Why does the ketone carbonyl group react in preference to the ester carbonyl? Is it something to do with the resonance occurring into the ester carbonyl from the oxygen? but how does this make the ...
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268 views

Electrophilic substitution in phenyl alkyl ether

Phenylalkyl ethers undergo usual halogenation in the benzene ring, e.g., anisole undergoes bromination with bromine in ethanoic acid even in the absence of iron (III) bromide catalyst. Why do we use ...
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356 views

How to calculate minimum temperature of a reaction?

For burning ethanol (its reaction with oxygen), we need a minimum activation energy (a minimum temperature) to start the reaction. Is it possible to calculate what are the minimum temperatures ...
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283 views

Why are trifluoromethyl diazirines so stable?

Why are trifluoromethyl diazirines so stable? Trifluoromethyl diazirines stability is well documented, however I am yet to find an explanation of why... Can it be homoaromatic or even aromatic? 2 pie ...
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272 views

Primary amine versus phosphoramidate reactivity with succinate esters

I have posted two reactions below. The top reaction is well known and occurs readily and near quantitatively (e.g. in protein modification), while the bottom reaction to my knowledge does not exist in ...
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27 views

Which is more reactive in E1, benzyl or allyl

I'm don't know the english terminology for chemistry so sorry for probably butchering some terms. My question is, which of these is more reactive in an E1 reaction: The bottom two are the ...
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38 views

Red Compound from Glycine and Glycerol?

I got an unexpected reaction which I'm trying to explain to myself: I mixed 10 parts glycerol with 1 part glycine at ~90C and to my great surprise the mixture turned from transparent to a tint of red. ...
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37 views

Why can't Grignard reagents react like Organolithium does (with acids)?

I'd read yesterday that Grignard reagents can't give ketones on reaction with carboxylic acids. It is because of the fact that Grignard reagent is a "super-base", and it will deprotonate the ...
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105 views

Why is the top SN2 reaction faster? (Molecular Orbital Theory)

I'm having trouble understanding why the top SN2 reaction proceeds faster. I know that benzylic and allylic halides react faster in SN2 reactions than non-conjugated halides. I think it's because the ...
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38 views

Is Gibbs energy minimized for processes at constant temperature are pressure only?

I've had this doubt for quite a while, This link https://chem.libretexts.org/Bookshelves/Physical_and_Theoretical_Chemistry_Textbook_Maps/Map%3A_Physical_Chemistry_for_the_Biosciences_(Chang)/04%...
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81 views

What happened to the Klopman - Salem equation?

I am relatively new and interested in the field of theoretical chemistry. I just stumpled across the Klopman - Salem equation (https://en.wikipedia.org/wiki/Klopman-Salem_equation). In daily life, ...
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390 views

Mechanism of Bis-decarboxylation of α,β-dicarboxylic acid

According to an internal test series in FIITJEE, it was given that the following compound decarboxylates on heating, I know that β-keto acids undergo decarboxylation on heating, but I was not sure ...
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207 views

How to predict and measure excess values of reactivity ratios for copolymerization with three monomers?

I ask this question because I haven't found interesting literature on the subject and I would like to know if my way to think is good or pure bullshit. Also the question is quite long because I have ...
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214 views

Requirement of different reagents for bromination of different substituted benzene rings

Consider the bromination reactions of phenol and anisole. We know that the former can be brominated by aqueous bromine, while the latter requires the catalyst $\ce{FeBr3}$ instead. Our teacher said ...
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64 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[...
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220 views

Why is cyclopropylmethyl radical opening so fast?

Ring opening of the cyclopropylmethyl radical is reliable and fast, and so has been used as a radical trap and a radical clock. Could someone please explain what exactly makes this reaction so fast, ...
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116 views

Material for melting metal oxides

I am constructing an apparatus for high temperature, strong alkaline melts (metal melts), with extremely high oxygen rich environments. Here what I have so far. Iridium is a good candidate - is it ...
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272 views

Why are copper, iron and lead so common in everyday use?

Copper, iron and lead are commonly used around the world in construction, for pipes and in electrical wiring. Why are these used instead of zinc and magnesium?
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81 views

What does the following sentence mean - “Li is least reactive but the strongest reducing agent among all alkali metals”

Isn't it contrasting? Is reactivity only concerned with kinetics of reaction ? PS - I am a high school student, probably I might be missing small detail!
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102 views

Are there any Endothermic Pyrophoric Substances?

I've recently been reading about pyrophoric materials, specifically as they relate to rocketry, and this made me curious if there are any substances which are the complete opposite of pyrophoric. ...