Using your reaction roadmap as a guide, show how to convert propane into butyronitrile. You must use propane and sodium cyanide as the source of all of the carbon atoms in the butyronitrile product. Show all reagents and all molecules synthesized along the way. NaCN Propane Sodium cyanide Butyronitrile

Using your reaction roadmap as a guide, show how to convert propane into butyronitrile. You must use propane and sodium cyanide as the source of all of the carbon atoms in the butyronitrile product. Show all reagents and all molecules synthesized along the way. NaCN Propane Sodium cyanide Butyronitrile

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

5 In the Fischer esterification reaction, a carboxylic acid reacts with an excess of alcohol in acidic conditions to form an ester. During the reaction the sp2 hybridized carbonyl carbon of the acid forms an sp3 hybridized intermediate before returning to sp² hybridization in the product. Draw the structure of the neutral sp³ hybridized intermediate and the ester product in the reaction between pentanoic acid and n-propanol. pentanoic acid + n-propanol Draw the neutral sp³ intermediate. Select Draw Templates More C H O H* propanol neutral sp³ intermediate Erase Draw the ester product. ester product Select Draw Templates More C H O Erase
calculate the theoretical yield of a reaction( in grams) between 5mmol N,N-diethylethanolamine and 5mmol 4-nitrobenzoyl chloride mw 4-nitrobenzoyl chloride: 185.56 g/mol mw N,N-diethylethanolamine: 117.9g/mol
Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons 1) NaNH2, NH3() NaBr + 2) CHзCH2CH2Br
Step 1: The carboxylic acid contains six carbons and the starting material should be an alkyl halide of five carbons or less, so you should look for a method of generating carboxylic acids by adding a carbon. One method of synthesizing carboxylic acids is from the hydrolysis of nitriles, which can be formed by substitution of alkyl halides. Identify the structure that contains a nitrile. OCH₂CH=NH OCH,CEN RCH=CHNH, OCH, CH₂NH,
What reagents would be needed to complete the following reaction? H2 CH3 CH3 H2/Pd AIC13/CH3CI HNO3/H2SO4 CH3CH2OH/H2O
Give the reagents or product(s) for each of the following reactions: Br LOH HBr NaH A da