Answer:
B. To change from a liquid state to a solid state is called Freezing
In 1 mol of CH3OH, you have 4 H-atoms (because 3 H-atoms
are attached to the C-atom, and one H-atom in the OH group). That means
in 0.500 mol of CH3OH, you have 2 H-atoms since it is halved. And then we have Avogadro's constant: 6.02 * 1023.
The question asks for how many hydrogen atoms there are in 0.500 mol CH3OH. Using the numbers that we have (Avogadro's constant and no. of H-atoms), the answer of the question will be something like:
<span>H-atoms in CH3OH = 2 * 6.02 * </span>1023<span> = ~1.2 * 10</span>24
<h3>
Answer:</h3>
5.55 mol C₂H₅OH
<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>
- Reading a Periodic Tables
- Moles
<u>Stoichiometry</u>
- Using Dimensional Analysis
- Analyzing Reactions RxN
<h3>
Explanation:</h3>
<u>Step 1: Define</u>
[RxN - Balanced] C₆H₁₂O₆ → 2C₂H₅OH + 2CO₂
[Given] 500. g C₆H₁₂O₆ (Glucose)
[Solve] moles C₂H₅OH (Ethanol)
<u>Step 2: Identify Conversions</u>
[RxN] 1 mol C₆H₁₂O₆ → 2 mol C₂H₅OH
[PT] Molar mass of C - 12.01 g/mol
[PT] Molar Mass of H - 1.01 g/mol
[PT] Molar Mass of O - 16.00 g/mol
Molar Mass of C₆H₁₂O₆ - 6(12.01) + 12(1.01) + 6(16.00) = 180.18 g/mol
<u>Step 3: Stoichiometry</u>
- [DA] Set up conversion:

- [DA} Multiply/Divide [Cancel out units]:

<u>Step 4: Check</u>
<em>Follow sig fig rules and round. We are given 3 sig figs.</em>
5.55001 mol C₂H₅OH ≈ 5.55 mol C₂H₅OH
The person above me is correct I took a test on this so it’s the right answer
Answer:
None of these
Explanation:
Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.
Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :
Step -1 : Generation of stable carbocation.
Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.
Step-2: Attack of the ring to the carbocation
The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.
The product formed is shown in mechanism does not mention in any of the options.
So, None of these is the answer