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lutik1710 [3]
3 years ago
12

The reaction in which methane is burned, CH4 +202 --> 2H20 + CO2, is an example of a

Chemistry
1 answer:
alexira [117]3 years ago
8 0

Answer: Combustion

Explanation:

Methane gas or natural gas is the hydrocarbon that reacts with oxygen as shown below: CH4 + 2O2 → CO2 + 2H2O There are two types of combustion reactions: complete and incomplete combustion. Therefore there are four products, carbon dioxide, water, carbon, and carbon monoxide.

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Which of the following series of isoelectronic ions (Mg²⁺, N³⁻, F⁻, Si⁴⁺) has the ionic radii in order of largest to smallest? A
Rom4ik [11]

Answer:

Option (d) is correct

N³⁻ > F⁻ > Mg²⁺ > Si⁴⁺

Explanation:

Total electrons for all the species = 10

So these are <u>iso electronic</u> with each other.

We know

Ionic radii ∝ \frac{Magnitude of Negative Charge}{Magnitude of Positive Charge}

  • Si⁴⁺ has 14 protons and 10 electrons
  • Mg²⁺ has 12 protons and 10 electrons
  • N³⁻ has 7 protons and 10 electrons
  • F⁻ has 9 protons and 10 electrons
  • Iso electronic species with greatest number of protons have small size and vice versa.
  • So Si⁺⁴ have smallest size and N³⁻ have largest in size
4 0
3 years ago
Describe at least three ways our understanding of the atom has changed overtime?
myrzilka [38]

Answer:

multitide of uses (drinking, cleaning, cooking, transportation). Without water we would not survive. -Lead atoms bond together and they make up the lead that we use as a pencil. -Copper atoms, aluminum atoms, nickel atoms, etc., all make up metal which is used for a variety of things in everyday life.

Explanation:

7 0
3 years ago
List and explain the four most important factors that control the relative reactivity of a carbonyl-containing functional group
ioda

Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.

Discussion:

1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.

2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.

3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.

4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.

Learn more about carbonyl here:

brainly.com/question/21440134

#SPJ4

8 0
1 year ago
Lithium diisopropylamide (LDA) is used as a strong base in organic synthesis. LDA is itself prepared by an acid-base reaction be
kakasveta [241]

Explanation:

Lithium diisopropylamide (LDA) is used in many organic synthesis and is a strong base. It is prepared by the acid base reaction of N,N-diisopropylamine ( [(CH₃)₂CH]₂NH ) and butyllithium ( Li⁺⁻CH₂CH₂CH₂CH₃ ).

The equation is show below as:

[(CH₃)₂CH]₂NH + Li⁺⁻CH₂CH₂CH₂CH₃  ⇒  [(CH₃)₂CH]₂N⁻Li⁺  + CH₃CH₂CH₂CH₃

N,N-diisopropylamine ( [(CH₃)₂CH]₂NH ) is a weaker acid and hence,  LDA ( [(CH₃)₂CH]₂N⁻Li⁺ ) is stronger base. (Weaker acid has stronger conjugate base)

Butyllithium ( Li⁺⁻CH₂CH₂CH₂CH₃ ) is a very strong base and hence, butane ( CH₃CH₂CH₂CH₃ ) is a very weak acid. (Strong base has weaker conjugate acid)

5 0
3 years ago
A detailed explanation, one paragraph of the colligative property being discussed and why that property changes the way that it
levacccp [35]
<span>
You can do it on the icing of roads, reverse osmosis for desalination of water, dissolved CO2 in soda cans, osmotic pressure involving blood vessels and IV solutions, etc.</span>
6 0
3 years ago
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