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larisa [96]
3 years ago
14

Using ammonia, show how Bronsted and Lowry improved the defination of acids and bases

Chemistry
1 answer:
emmasim [6.3K]3 years ago
5 0
Ammonia what is that
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Purest form of carbon is
vladimir2022 [97]

Answer:

Obtención. El carbono se encuentra - frecuentemente muy puro - en la naturaleza, en estado elemental, en las formas alotrópicas diamante y grafito. El material natural más rico en carbono es el carbón (del cual existen algunas variedades). Grafito: Se encuentra en algunos yacimientos naturales muy puro.

4 0
3 years ago
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When doing a titration what is the equivalency point of the neutralization reaction?
KengaRu [80]
The equivalency point is at the point of the titration where the amount of titrant added neutralize the solution. When it’s a strong acid strong base titration, the equivalence point will be 7. When it is a weak acid strong base, the equivalence point it more basic (the exact number depends on what acid and base you use). And when it is a strong acid weak base, the equivalence number is more acid (the exact number depends on what acid and base you use). Hope this helps!
3 0
3 years ago
What is the formula for this ionic formula ba 0
cestrela7 [59]

Answer:

BaO

Explanation:

The barium oxide chemical formula is BaO. The molar mass is 153.33 g/mol. The molecule is formed by one barium cation Ba2+ and one oxide anion O2-. Both ions are bound by one ionic bond.

3 0
2 years ago
Which is NOT a way that Carbon is released in to the atmosphere?
amid [387]

Answer:

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Explanation:

8 0
2 years ago
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In the reduction of 4-tert-butylcyclohexanone with sodium borohydride, the major product has the tert-butyl group in the equator
Evgen [1.6K]

Answer:

Axial position

Explanation:

In the reduction of 4-tert-butylcyclohexanone with sodium borohydride, the major product has the tert-butyl group in the equatorial position and the alcohol in the axial position.

The reason for this is that, axial bonds are parallel to each other. If  substituents are larger than hydrogen, they experience a greater steric crowding in axial compared to the equatorial position. Therefore, many substituted cyclohexane compounds prefer a conformation in which the larger substituents are in equatorial position.

8 0
3 years ago
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