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marshall27 [118]
3 years ago
15

Why does hydrogen have a -1 oxidation state in the compound NaH?

Chemistry
1 answer:
ruslelena [56]3 years ago
6 0

your answer will be :

B. <u>Na has a lower</u> <u>electronegativity than H</u>

because Na belongs to alkali metals which are least electronegative (most electro positive) but hydrogen is a non metal, it has higher electronegativity as compared to metals like Sodium (Na).

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The inhibition caused by the final end product of a reaction is called
Troyanec [42]

Answer:

Non competitive inhibition

Explanation:

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During enzymatic catalysis, the active sites could be occupied by the very same products' molecules turning out into an inhibition (the reaction starts to slow down since to active places are available for the reagents to react). Nonetheless this inhibition is not competitive as long as the product does not react due to the active sites it is occupying.

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5 0
3 years ago
b. Determine the molecular formula of a molecule with an empirical formula NH2and a molar mass of 32 g/mol.
VladimirAG [237]
I'm taking this lesson now, so imma help u ( if u need anything else ask me)

so given Molar mass= 32 g/mol
molar mass= (empirical formula) n
32 = (14x1 + 2x1) n
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so, molecular formula= N2H4
5 0
3 years ago
True or False? Not all compounds will dissolve in water.
In-s [12.5K]

Answer:

False

Explanation:

Polar molecules and ionic compounds dissolve in water, not nonpolar molecules

4 0
3 years ago
(a) What property is used today for the order of the elements?
Gennadij [26K]

Answer:

I feel as though you are missing information to this question.

Explanation:

elements on the periodic table, today, are arranged based on physical properties, such as valence electrons, atomic mass, etc.

3 0
3 years ago
Aldehydes and ketones react reversibly with two equivalents of alcohol in the presence of an acid catalyst to give acetals. Alco
kozerog [31]

Answer:

Aldehyde and ketone both react with alcohols (2 equivalent) in the presence of acid catalyst to give acetals.

Explanation:

Alcohols are poor nucleophiles and so protonation of the carbonyl oxygen used to make the carbonyl carbon a stronger electrophile. Addition of the first equivalent of alcohols gives a hemiacetal,

Addition of the second equivalent of alcohol is accompanied by loss of one molecule water to yield the produce acetal.

6 0
3 years ago
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