When two functional groups are capable of reacting with same reagent but we want only one functional group to undergo reaction then we protect the other functional group by using protecting group which can be removed by acidic hydrolysis later after completion of reaction of desired reaction.
Incorporate the protection and deprotection of ketones, aldehydes, and alcohols in syntheses. 6. The following reaction...
write three reaction in the synthesis of alcohols, aldehydes and ketones using the reducing agent LiAlH4
Alcohols, Aldehydes, and Ketones Report Sheet c. Oxidation of Alcohols C.3 C.2 Condensed Structural Formula Classification C.1 Color Change with Cro - yes Alcohol C.4 Oxidation Product (if reaction takes place) Ethanol Aldehyde yes Primary 2-Propanol yes Secondary Ketone 2-Methyl- 2-propanol tertiary Cyclohexanol Questions and Problems Q.2 Write the product of the following reactions (if no reaction, write NR): CH2CH2CH2OH CH3CH2CH=0
6) a)Write structural formulas and provide IUPAC names for all of the isomeric aldehydes and ketones that have the molecular formula C6H12O. Include stereoisomers. b) Circle the isomers in part a that yield chiral alcohols upon reaction with sodium borohydride. c) Circle the isomers in part a that yield chiral alcohols upon reaction with methyl magnesium iodide.
College Chem I CHE 132 Alcohols, Aldehydes, & Ketones Draw the structure of the product for each reaction. Name the reactant and the product. + Hz OH ciH 2 netng gelopentanol +HNi Ciy CHy c) CCyC нос 180 Ho e) CH5-CH-CH- PE CHS CAS u-Ca-aes CHS
Alcohols, Aldehydes, and Ketones Report Sheet Q.5 Indicate the test results for each of the following compounds in the iodoform test and in the Benedict's test: lodoform Test Benedict's Test CH.CCH.CH CH,CH CH3CH2CCH,CH, 0 0 CH3CCH.CH Q.6 Two compounds, A and B have the formula of C3H,0. Determine their condensed structural formulas and names using the following test results. a. Compound A forms a red-orange precipitate with Benedict's reagent, but does not react with iodoform. b. Compound B forms a...
8. Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. The synthesis should not take more than three or four reactions. At least one of the reactions should come from the aldehydes and ketones chapter. (6 pts) a) CO2H b)
Question 5 Aldehydes react with CrO 3/H 30 O A. ketones. to form B. carboxylic acids. C. alcohols D. alkanes. Moving to another question will save this response A Moving to another question will save this response. Question 4 The Williamson ether synthesis requires that the alkyl halide must be either a OA methyl or primary alkyl halide. OB. secondary or tertiary alkyl halide. OC methyl or tertiary alkyl halide. O D. primary or a secondary alkyl halide. A Moving...
Chem 202, Autumn 2019 Homework Packet 10 (Aldehydes and Ketones) 6. Reaction Fill-ins. Predict the product(s) OR starting material of the following reactions. Put your answers in the indicated boxes. NaOCI CH3COOH 1. NaBH4 2. H3O+ MgBr 2. Hz0+ H2Cr04 e. YYOH HyCros NaOCI OH CH3COOH 4 Page
pre-Laboratory Questions-EXP 6 Name: Qualitative Analysis of Ketones and Aldehydes Due before lab begins. Answer in space provided. 1. Give the structure of the organic product of the reaction of phenylacetaldehyde with the following.(give the names of the products). (a) Tollens' reagent (b) Jones' reagent 2. Write a complete mechanism of reaction of 2,4-dinitrophenylhydrazine with acetaldehyde.
This experiment was based on Aldol-dehydration reaction using unknown aldehydes and ketones. We carried out an aldol condensation between an unknown aldehyde and an unknown ketone. Here are the list of possible unknown aldehydes and ketones that were used. Here is the NMR of the final product. Please predict the structure given the melting point is 163 degrees Celsius. The analysis of the 1H NMR spectrum should include a detailed assignment of each of the NMR resonances to the protons...