Answer:
Stoichiometric Coefficients
The balanced equation makes it possible to convert information about one reactant or product to quantitative data about another element. Understanding this is essential to solving stoichiometric problems
Explanation:
Answer:
Ammonia > Urea > Ammonium nitrate > Ammonium sulphate
Explanation:
Percentage by mass of nitrogen in NH3:
Molar mass of NH3= 17 g/mol
Hence % by mass = 14/17 × 100 = 82.35%
% by mass of NH4NO3
Molar mass of NH4NO3 = 80.043 g/mol
Hence; 28/80.043 × 100 = 34.98%
% by mass of (NH4)2SO4;
Molar mass of (NH4)2SO4= 132.14 g/mol
Hence; 28/132.14 × 100 = 21.19%
% by mass of CH4N2O
Molar mass of urea = 60.0553 g/mol
Hence 28/60.0553 × 100 = 46.62%
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Answer:</h3>

<h3>
General Formulas and Concepts:</h3>
<u>Math</u>
<u>Pre-Algebra</u>
Order of Operations: BPEMDAS
- Brackets
- Parenthesis
- Exponents
- Multiplication
- Division
- Addition
- Subtraction
<u>Chemistry</u>
<u>Atomic Structure</u>
- Avogadro's Number - 6.022 × 10²³ atoms, molecules, formula units, etc.
<u>Stoichiometry</u>
- Using Dimensional Analysis
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Explanation:</h3>
<u>Step 1: Define</u>
6.022 × 10²² atoms Fe (iron)
<u>Step 2: Identify Conversions</u>
Avogadro's Number
<u>Step 3: Convert</u>
- Set up:

- Divide:

Answer: It is 5450 mL
Explanation: There are 1000 mL in every L and then there is an extra 450 so just add that at the end
Answer:but-1-ene
Explanation:This is an E2 elimination reaction .
Kindly refer the attachment for complete reaction and products.
Sodium tert-butoxide is a bulky base and hence cannot approach the substrate 2-chlorobutane from the more substituted end and hence major product formed here would not be following zaitsev rule of elimination reaction.
Sodium tert-butoxide would approach from the less hindered side that is through the primary centre and hence would lead to the formation of 1-butene .The major product formed in this reaction would be 1-butene .
As the mechanism of the reaction is E-2 so it will be a concerted mechanism and as sodium tert-butoxide will start abstracting the primary hydrogen through the less hindered side simultaneously chlorine will start leaving. As the steric repulsion in this case is less hence the transition state is relatively stabilised and leads to the formation of a kinetic product 1-butene.
Kinetic product are formed when reactions are dependent upon rate and not on thermodynamical stability.
2-butene is more thermodynamically6 stable as compared to 1-butene
The major product formed does not follow the zaitsev rule of forming a more substituted alkene as sodium tert-butoxide cannot approach to abstract the secondary proton due to steric hindrance.