Limiting Reagent & Percent Yield | Wyzant Ask An Expert

Subject ZIP Search Search Find an Online Tutor Now Ask Ask a Question For Free Login Organic Chemistry Limiting Reagent & Percent Yield

5. Determine the limiting reagent and calculate the percent yield of isopentyl acetate in the g reaction. The density of acetic acid is 1.049 gmL. You must show all work for credit. H2SO4 acetic acid C2H402 isopentyl alcohol CH120 isopentyl acetate C,H1402 water To 11.10g of isopentyl alochol in a dry 150-mL round bottom flask, was added 24.5mL of acetic acid and a catalytic amount of H2SO4 (5.0 mL). The reaction mixture was refluxed for 30 minutes. The reaction mixture was then allowed to cool and washed with 5% sodium bicarbonate and water. The crude product was dried over sodium sulfate. It smelled strongly of bananas. The crude product was distilled to yield 7.102g of isopentyl acetate

Follow 1 Add comment More Report

1 Expert Answer

Best Newest Oldest By: Best Newest Oldest

You need correct molecular formulas before working on the math!! C5H12O and C7H14O2 are the alcohol and acetate. I'm using rounded integer numbers for molar mass; you can refine and show your calculations of molar mass for the assignment.

Balanced equation: C5H12O + C2H4O2 ---> C7H14O2 + H2O

Moles 11.10/88 24.5 X 1.049/60 7.102/130 (actual)

0.126 0.428 0.0546

Since the reactants and products are all in 1:1 ratio, it is easy to see that the limiting reagent is C5H12O, and the theoretical yield will be 0.126 mol. Since the actual yield is 0.0546, the percent yield is

100 X 0.0546/0.126 = 43.3%, rounded off.

Upvote 0 Downvote Add comment More Report

Still looking for help? Get the right answer, fast.

Ask a question for free

Get a free answer to a quick problem. Most questions answered within 4 hours.

OR

Find an Online Tutor Now

Choose an expert and meet online. No packages or subscriptions, pay only for the time you need.

¢ € £ ¥ ‰ µ · • § ¶ ß ‹ › « » < > ≤ ≥ – — ¯ ‾ ¤ ¦ ¨ ¡ ¿ ˆ ˜ ° − ± ÷ ⁄ × ƒ ∫ ∑ ∞ √ ∼ ≅ ≈ ≠ ≡ ∈ ∉ ∋ ∏ ∧ ∨ ¬ ∩ ∪ ∂ ∀ ∃ ∅ ∇ ∗ ∝ ∠ ´ ¸ ª º † ‡ À Á Â Ã Ä Å Æ Ç È É Ê Ë Ì Í Î Ï Ð Ñ Ò Ó Ô Õ Ö Ø Œ Š Ù Ú Û Ü Ý Ÿ Þ à á â ã ä å æ ç è é ê ë ì í î ï ð ñ ò ó ô õ ö ø œ š ù ú û ü ý þ ÿ Α Β Γ Δ Ε Ζ Η Θ Ι Κ Λ Μ Ν Ξ Ο Π Ρ Σ Τ Υ Φ Χ Ψ Ω α β γ δ ε ζ η θ ι κ λ μ ν ξ ο π ρ ς σ τ υ φ χ ψ ω ℵ ϖ ℜ ϒ ℘ ℑ ← ↑ → ↓ ↔ ↵ ⇐ ⇑ ⇒ ⇓ ⇔ ∴ ⊂ ⊃ ⊄ ⊆ ⊇ ⊕ ⊗ ⊥ ⋅ ⌈ ⌉ ⌊ ⌋ 〈 〉 ◊

RELATED TOPICS

Science Chemistry Biochemistry Chemical Reactions Acid Base reactions Resonance Organic Acid Base Stability Isomers ... Inorganic Chemistry Chemical Changes Chemical Formula Chemistry Lab Carbocation Aromatic Compounds Halides Reaction Mechanism Chirality Carbonyl Compounds

RELATED QUESTIONS

Why does boiling point increase start to diminish when alkanes get larger?

Answers · 3

how do you find a chemical shift of an unknown arene?

Answers · 2

how many grams of barium sulfate will be formed from 60.0 g of barium nitrate and 2.0 grams of sodium sulfate

Answers · 3

Resonance Contributor

Answers · 2

Consider the substitution reaction that takes place when (R)-3-bromo-3-methylhexane is treated with sodium methoxide. Which of the following would be true?

Answers · 3

RECOMMENDED TUTORS

Lohith D.

5.0 (487)

Anna A.

5.0 (608)

Kara T.

5.0 (819) See more tutors

find an online tutor

  • Organic Chemistry tutors
  • Chemistry tutors
  • Physical Chemistry tutors
  • AP Chemistry tutors
  • Biochemistry tutors
  • Microbiology tutors
  • Chemical Engineering tutors
  • Biology tutors

Từ khóa » Ch3cooh+c5h12o+h2so4