Use the following atomic weights and quantities to calculate the overall % yield of 4-carboxamide-4'-pentyllbiphenyl. Remember that your yield must be based on the stoichiometry(Look back to the mechanism question for the correct stoichiometry of this reaction!), the limiting reagent, and that grams must be converted to moles. Filling out most of the chart willhelp. Give only two significant digits in your answer. If after rounding the answer is a whole number, do not include a decimal point.C = 12, H = 1, CI = 35.5, N = 14, 0 = 16formulaformula weightmillilitersdensitygramsmoles4-chlorocarbonyl-4'-pentylbiphenyl 14.8 M ammonium hydroxide →>> 4-carboxamide-4'-pentylbiphenyl1.7560.8381.440Answer:% yield?

Answered: Use the following atomic weights and…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.63P

See similar textbooks

Similar questions

3. Consider the pictured acid-catalyzed esterification. a) What is the limiting reagent in the reaction? and explain how you chose the limiting reagent, including any performed calculations. b) What is the theoretical yield (in g) of octyl acetate? c) Assume that your isolated yield of octyl acetate was 5.00 mL, calculate the percent yield of the reaction.
Explain why benzocaine precipitates during the neutralization.
Does it safe to use this product on face during the morning? And Can we use it everyday both in case of using before bed time and in the morning? This product has lists of ingredients below (descending order)…. Hydroxyethylpiperazine ethane sulfonic Acid Glycolic Acid Alcohol denat. Pentylene glycol Sodium hydroxide Citric Acid Ascorbyl glucoside
The theoretical yield of 1-methylcyclohexene in moles(from 2-methylcyclohexanol amount of 2.239 gram). The theoretical yield of 1-methylcyclohexene in moles is 0.01961. 1. What is the corrected actual yield(% Relative Area for 1-methylcyclohexene is 82.81%)? The theoretical yield of 1-methylcyclohexene in moles is 0.01961. 2. . What is the calculation of the %yield of 1-methylcyclohexene?
4-chloro-3,4-dimethylnonan-1-amine On a page titled Incorrect Separation Scheme print the incorrect separation schemeprovided for your molecule on Blackboard. The top of the separation scheme shows whatother compound is mixed with your molecule. Assume for the purposes of this assignmentthat both compounds are solid at room temperature. Also assume that both compounds aresoluble in ether, except ionic compounds. The goal of the separation is the isolate each ofthe two compounds from the mixture.o Below the incorrect separation scheme write a discussion of this incorrect schemeidentifying all of the mistakes in the separation scheme. Keep in mind that therewill be more than one mistake in the scheme.o For each mistake, give a detailed, scientific explanation of why it is incorrect.
Assuming that benzaldehyde is the limiting reagent for the synthesis of stilbene, that stilbene is the limiting reagent for the synthesis of stilbene dibromide, and that stilbene dibromide is the limiting reagent for the synthesis of diphenylacetylene; what is the overall % yield of diphenylacetylene from benzaldehyde given the percentage yield of each step of the reaction sequence as follows? Give only two significant digits. If the answer is a whole number with two digits, do not include the decimal. benza Idehy de Notes: 66% stil be ne 23% stilbene dibromi de 66% dipheny lacetyle ne
Assuming that benzaldehyde is the limiting reagent for the synthesis of stilbene, that stilbene is the limiting reagent for the synthesis of stilbene dibromide, and that stilbene dibromide is the limiting reagent for the synthesis of diphenylacetylene; what is the overall % yield of diphenylacetylene from benzaldehyde given the percentage yield of each step of the reaction sequence as follows? Give only two significant digits. If the answer is a whole number with two digits, do not include the decimal. 52% 87% benzaldehyde → stilbene → stilbene dibromide 41% Answer: diphenylacetylene Notes: For our multi-step synthesis we cannot just calculate the yield based on starting amount of benzaldehyde and final amount of diphenylacetylene because your group may have been supplemented with commercial material at one or more steps. In truth most chemist use an excess of the least expensive reagent to increase their yield. So in our case benzyltriphenylphosphonium chloride should probably be our…
Methyl benzoate can be synthesized by a Fisher Esterification reaction, and then this ester can be used as a starting material in the grignard synthesis of triphenyl carbinol. Suppose that in the synthesis of methyl benzoate, a student started with 12 grams of benzoic acid and 29.86 ml of methanol. After finishing the preparation of the ester, 7.63 grams of methylbenzoate was obtained, and the benzoic acid reacted completely. What is the percent yield of the ester? ( density methanol = 0.791 g/ml, methanol = 32.04 g/mol, methyl benzoate = 136.15 g/mol, benzoic acid = 122.12 g/mol )
What reagent would you use to distinguish between the aldehydes and ketones and indicate what you would observe
Explain the general procedure for the laboratory preparation of the synthesis of Aniline from benzoic acid. (paragraph form) Explain the chemistry behind the synthesis of Aniline from benzoic acid. (paragraph form)
Write the reaction that could produce propanoyl chloridefrom from any organic reagents.
find the molecular and empirical formula of the alkene when it is known that during the action of 0.672 liters of the same alkene under normal conditions with chlorine were formed 3.39 grams of dichlorinated product

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Chemistry for Today: General, Organic, and Bioche…

Chemistry

ISBN:

9781305960060

Author:

Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Chemistry for Today: General, Organic, and Bioche…

Chemistry

ISBN:

9781305960060

Author:

Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:

Cengage Learning

Macroscale and Microscale Organic Experiments

Chemistry

ISBN:

9781305577190

Author:

Kenneth L. Williamson, Katherine M. Masters

Publisher:

Brooks Cole

SEE MORE TEXTBOOKS