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defon
3 years ago
9

Describe the De Borglie's hypothesis​

Chemistry
1 answer:
Advocard [28]3 years ago
3 0

Answer:

The De Broglie hypothesis proposes that all matter exhibits wave-like properties and relates the observed wavelength of matter to its momentum. After Albert Einstein's photon theory became accepted, the question became whether this was true only for light or whether material objects also exhibited wave-like behavior.

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Please HELP will give Brainliest!!!!!
dedylja [7]
4 mol / 205g H2O = 4/.205 = 19.5 mol/kg boiling point = 100 + 19.5 • 0.51 = 109 ºC
7 0
4 years ago
Why does iron have no oxidation state corresponds to loss of all it's valence electrons?
olganol [36]

Answer:

When an element loses an electron, its oxidation number increases.

Explanation:

The oxidation number of an element indicates the hypothetical charge of an atom in a compound. It is hypothetical because, in the context of a compound, the elements may not necessarily be ionic. When the number of electrons associated with an atom changes, its oxidation number also changes. When an element loses an electron, its oxidation number increases.

7 0
4 years ago
The reason your classmate cannot find the compound in a chemical reference manual is that 2,4-diethyl-4-ethoxyhexane is the inco
Georgia [21]

Answer:

3-ethoxy-3-ethyl-5-methylheptane

Explanation:

In this case, we have to identify the longest chain of carbon in this case the longest chain is made with 7 carbons. Then we have to assign carbon 1. In this case, carbon 1 is the one nearest to the ethoxy group. With this in mind, we will have a methyl on carbon 5, a methyl on carbon 3 and an ethoxy group in carbon 3, so the name would be 3-ethoxy-3-ethyl-5-methylheptane.

See figure 1

I hope it helps!

8 0
3 years ago
A chemical reaction happens in three steps.
oee [108]
Steps 1 and 3 are correct rate
7 0
3 years ago
The first mechanistic step in the direct reaction of an amine with a carboxylic acid to produce an amide is ________.
Effectus [21]

Answer:

The first step is - option A) an acid base reaction.

Explanation:

The direct reaction of a carboxylic acid with an amine to form an amide is expected to be difficult as it would deprotonate the carboxylic acid and make a nonreactive carboxylate.

The first step in this reaction would be an acid - base reaction as protonation of the carbonyl carbon, that involves the interchange of proton in between electric charge or neutral compound, it is also known as protonation or deprotonation. The acid base reaction is followed by the nucleophilic attack on the carbonyl carbon.

Thus, The first step is - option A) an acid base reaction.

5 0
3 years ago
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