Answer:
Cancel out CO because it appears as a reactant in one intermediate reaction and a product in the other intermediate reaction.
Explanation:
The CO appears twice hence in he intermediate reaction it only forms path of the enabling reagents and it further reacts to form the final product. Accounting for the CO in the intermediate reaction that undergoes further reaction will impact on the stoichiometry of the reaction.
Answer:
There is a relationship between the strength of an acid (or base) and the strength of its conjugate base (or conjugate acid): The stronger the acid, the weaker its conjugate base. The weaker the acid, the stronger its conjugate base. The stronger the base, the weaker its conjugate acid.
explanation
The strength of an acid and a base is determined by how completely they dissociate in water. Strong acids (like stomach acid) break down or dissociate in water. Weak acids maintains their protons in water.
<h2>
Answer:True</h2>
Explanation:
Heterogeneous mixture is a mixture with non-uniform composition.
The properties of the mixture like concentration may change for different parts of the mixture.
Colloids contain solute particles of size 
.The presence of these particles makes the mixture heterogeneous.
Suspensions contain solute particles of size 
.These particles settle to the bottom of the mixture which makes the composition of the bottom different from the top.
So,colloids and suspensions are two types of heterogeneous mixtures.
The correct option is (b)
NaNH2 is an effective base. It can be a good nucleophile in the few situations where its strong basicity does not have negative side effects. It is employed in elimination reactions as well as the deprotonation of weak acids.Alkynes, alcohols, and a variety of other functional groups with acidic protons, such as esters and ketones, will all be deprotonated by NaNH2, a powerful base.Alkynes are deprotonated with NaNH2 to produce what are known as "acetylide" ions. These ions are powerful nucleophiles that can react with alkyl halides to create carbon-carbon bonds and add to carbonyls in an addition reaction.Acid/base and nucleophilic substitution are the two types of reactions.Using the right base, terminal alkynes can be deprotonated to produce a carbanion.A good C is the acetylide carbanion.The acetylide carbanion can undergo nucleophilic substitution reactions because it is a potent C nucleophile. (often SN2) with 1 or 2 alkyl halides with electrophilic C to create an internal alkyne (Cl, Br, or I).Elimination is more likely to occur with 3-alkyl halides.It is possible to swap either one or both of the terminal H atoms in ethylene (acetylene) to create monosubstituted (R-C-C-H) and symmetrical (R = R') or unsymmetrical (R not equal to R') disubstituted alkynes (R-C-C-R').
Learn more about NANH2 here :-
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