The red end of the spectrum.
<u>Answer:</u>
<em>The option a termed as precipitation reaction is incorrectly labelled.
</em>
<u>Explanation:</u>
The chemical reactions are classified based on the reactants used and products formed in a reaction. They are decomposition reaction, single displacement reaction, double displacement reaction, acid-base neutralisation reaction, precipitation reaction, combustion reaction, redox reaction and organic reaction.
Among these, the given options are labelled as precipitation and combustion reaction. The one which is labelled as combustion reaction is correct because combustion reactions occur in the presence of oxygen only and the products of combustion reaction should include water, oxygen or carbon and heat.
The other option which is labelled as precipitation reaction is incorrect because precipitation reaction occurs when an ionic substance will come out of a solution due to heating it or stirring it making the solubility of the ionic substance in a solution zero such that it will come out as solid and form a layer at the bottom of the solution.
But in this case all the products are in aqueous state, there is absence of any ionic substance in solid state, so the option which is labelled as precipitation reaction is incorrectly labelled.
Answer:
See the image 1
Explanation:
If you look carefully at the progress of the SN2 reaction, you will realize something very important about the outcome. The nucleophile, being an electron-rich species, must attack the electrophilic carbon from the back side relative to the location of the leaving group. Approach from the front side simply doesn't work: the leaving group - which is also an electron-rich group - blocks the way. (see image 2)
The result of this backside attack is that the stereochemical configuration at the central carbon inverts as the reaction proceeds. In a sense, the molecule is turned inside out. At the transition state, the electrophilic carbon and the three 'R' substituents all lie on the same plane. (see image 3)
What this means is that SN2 reactions whether enzyme catalyzed or not, are inherently stereoselective: when the substitution takes place at a stereocenter, we can confidently predict the stereochemical configuration of the product.
Answer:
cis-1-tert-butyl-3-methylcyclohexane will have a higher percentage of the diequatorial-substituted conformer when compared with the diaxialsubstituted conformer.
Explanation:
The two compound contain or have high stability with the substituent group is at equatorial position but the tert-betyl group in cis-1-tert-butyl-3-methylcyclohexane is larger than the methyl group in trans-1,4-dimethylcyclohexane.
Thus, the equatorial position will be more favorable for the substituent group in the cis-1-tert-butyl-3-methylcyclohexane, therefore having higher percentage of the diequatorial substituted conformer compared with that of diaxial-substituted conformer.
To determine the strength of potassium permanganate with a standard solution of oxalic acid.
