Question
I was wondering if anyone could help with finding the theoretical yield? i need to get the Limiting Reagent to find the theoretical yield. it would be appreciated thanks!

cyclohexanol MW: 110.16
cyclohexene MW: 82.14
Walol. 2. Cyclohexanol and especially cyclohexene are flammable liquids. Do not heating source in this experiment som stalo t
Experimental Procedure (macroscale) Add 20 mL of cyclohexanol and 5 mL of 85% phosphoric acid to a 50-ml round-bottom flask a
0 0
Add a comment Improve this question Transcribed image text
Answer #1

Here in this reaction, Cyclohexanol forms cyclohexene in the presence of phosphoric acid.

Cyclohexanol ==> cyclohexane ; catalyst = phosphoric acid

Hence only one reagent is available, Phosphoric acid is a catalyst. So limiting reagent is cyclohexanol.

Taken 20 mL of cyclohexanol, density = 0.960 g/mL

weight of taken cyclohexanol = volume x density

= 20 mL x 0.960 g/mL

weight of taken cyclohexanol = 19.2 g

Moles of cyclohexanol = weight of cyclohexanol taken/ molar mass of cyclohexanol

= 19.2 g/110.16 (g/mol)

Moles of cyclohexanol = 0.1743 mole

1 mole of Cyclohexanol gives 1 mole of Cyclohexene

110.16 g/mol of Cyclohexanol gives 82.14 g/mol of Cyclohexene

1 of Cyclohexanol gives 82.14 (g/mol)/110.16 (g/mol) of Cyclohexene

19.2 g of Cyclohexanol gives {82.14 (g/mol)/110.16 (g/mol)} x 19.2 g of Cyclohexene

19.2 g of Cyclohexanol gives 14.3163 g of Cyclohexene

Theoretical yield = 14.3163g

Add a comment
Know the answer?
Add Answer to:
I was wondering if anyone could help with finding the theoretical yield? i need to get...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • based on the amount of cyclohexanol used in the procedure, calculate the theoretical yield of cyclohexene...

    based on the amount of cyclohexanol used in the procedure, calculate the theoretical yield of cyclohexene product. show all work. info attached below ОН Н,РО,. H2SO + Н,о Procedure Cyclohexanol (10 g) is weighed into a 50 mL round-bottom three-necked flask, while avoiding getting the liquid on the ground-glass joint. To this is added 2.5 mL of 85% phosphoric acid along with two drops of sulfuric acid (again, avoiding getting the liquids on the joint) and a few boiling stones....

  • Rewrite the text in past tense Use only third person, passive voice, e.g.: “Thirty grams of...

    Rewrite the text in past tense Use only third person, passive voice, e.g.: “Thirty grams of naphthalene was added 50 mL of m-xylene in a 250 mL round bottomed flask.” Experimental Procedure 1. Set up a simple distillation apparatus. 2. Add 16 g (16.7 mL) of cyclohexanol and 4 mL of concentrated sulfuric acid to the round bottom flask. Caution: Sulfuric acid is highly corrosive. Use caution and appropriate personal protective equipment! 3. Mix contents thoroughly and connect to distillation...

  • The alcohol could easily be converted to a tosylate, a good leaving group, and a conventional sub...

    The alcohol could easily be converted to a tosylate, a good leaving group, and a conventional substitution reaction could have been performed instead of the nucleophilic aromatic substitution (NAS) reaction. Why was the NAS reaction the preferred method? (Hint : Look up the nucleophiles of both reactions on chemical manufacturing site.) Part A: Synthesis of (t)-N,N-dimethyl-3-phenyl-3-(4- trifluoromethylphenoxy)propanamine 1. To the 250-mL round-bottom flask (RBF) containing (t)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-...

  • The alcohol could easily be converted to a tosylate, a good leaving group, and a conventional...

    The alcohol could easily be converted to a tosylate, a good leaving group, and a conventional substitution reaction could have been performed instead of the nucleophilic aromatic substitution (NAS) reaction. Why was the NAS reaction the preferred method? (Hint : Look up the nucleophiles of both reactions on chemical manufacturing site.) Part A: Synthesis of (t)-N,N-dimethyl-3-phenyl-3-(4- trifluoromethylphenoxy)propanamine 1. To the 250-mL round-bottom flask (RBF) containing (t)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-...

  • You don’t have to tell me purpose. just where in procedure for each technique. Section/Instructor SN2...

    You don’t have to tell me purpose. just where in procedure for each technique. Section/Instructor SN2 Pre-lab (20 points) Answer on a separate piece of paper 1. (6 pts.) What is the purpose of the following experimental techniques and where in the procedure is each used? a. Heating under reflux b. Simple distillation c. Water wash d. Addition of COLD NAOH e. Saturated NaCl solution f. Addition of anhydrous sodium sulfate SN2 Reaction Procedure Set-Up: 100 mL RBF: 11.1 g...

  • Working on the questions at the end of this lab report (see above). I need help answering questio...

    Working on the questions at the end of this lab report (see above). I need help answering questions 2, 3, and 4 completely and thoroughly. Thank you! s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...

  • how do I get the molar ratios between NaBr, 1-butanol and H2SO4 used in the experiment...

    how do I get the molar ratios between NaBr, 1-butanol and H2SO4 used in the experiment sn2 reaction 1-bromobutane Moles: NaBr: 0.0275 Butanol: 0.0216 H2SO4: 0.00840 butanol is the limiting reagent Experiment: 08 The S2 Reaction: 1-Bromobutane Substitution nucleophilic bimolecular (SN2) reactions can be utilized to convert primary alcohols to corresponding halogens. In this experiment, 1-butanol is treated with a nucleophile (Br) to generate the corresponding 1-bromobutane. The nucleophile in this lab is generated from an aqueous solution of NaBr....

  • SYNTHESIS OF T-PENTYL CHLORIDE LAB Provide a stoichiometry table for the reaction being performed in this...

    SYNTHESIS OF T-PENTYL CHLORIDE LAB Provide a stoichiometry table for the reaction being performed in this lab. PROCEDURE Preparation oft-Pentyl Chloride In a 125-mL separatory funnel, place 10.0 mL of tert-pentyl alcohol (2-methyl-2- butanol, MW = 88.2, d = 0.805 g/mL) and 25 mL of concentrated hydrochloric acid (d 1.18 g/mL). Do not stopper the funnel. Gently swirl the mixture in the separa- tory funnel for about 1 minute. After this period of swirling, stopper the separatory funnel and carefully...

  • I need help with this post lab from Orgo. Anyone please help me. I have included...

    I need help with this post lab from Orgo. Anyone please help me. I have included the procedure from experiment, but let me know if there is anything to add on this. Thank you 1. Write the overall balanced chemical equation (not the mechanism) for the reaction you carried out in this experiment. Equation must be charge and mass balanced. Use structures not molecular formula. (3 pts) Part A Table 2: Complete this table (15 pts) 2-methyl cyclohexanol cycloalkene Molecular...

  • How can the NMP oxalate salt be converted back to NMP? Here is the procedure: PROCEDURES...

    How can the NMP oxalate salt be converted back to NMP? Here is the procedure: PROCEDURES Part A: Synthesis of (±)-N,N-dimethyl-3-phenyl-3-(4-trifluoromethylphenoxy)propanamine To the 250-mL round-bottom flask (RBF) containing (±)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-chlorobenzotrifluoride and 30 mL of dimethylacetamide (DMA). With stirring, add to this mixture 30 mL of 1.0 M potassium tert-butoxide (caustic alkali!) in tert-butyl alcohol using a syringe. Using a simple distillation apparatus, distill the mixture slowly, with...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT