
(a)
To determine: The accomplishment of given synthetic conversion.
Interpretation: The accomplishment of given synthetic conversion is to be stated.
Concept introduction: The metallic sodium is used for conversion of alcohols into sodium alkoxide. The further reaction of sodium alkoxide with an
(b)
To determine: The accomplishment of given synthetic conversion.
Interpretation: The accomplishment of given synthetic conversion is to be stated.
Concept introduction: Sodium hydroxide is used for the conversion of alkyl halide into primary alcohol. The conversion of a primary alcohol into
The Grignard reagent is prepared by reaction of an alkyl halide with metallic magnesium in the presence of THF (tetra hydro furan). The further reaction of prepared aldehyde with Grignard reagent in the presence of
(c)
To determine: The accomplishment of given synthetic conversion.
Interpretation: The accomplishment of given synthetic conversion is to be stated.
Concept introduction: The Grignard reagent is prepared by reaction of an alkyl halide with metallic magnesium in the presence of THF (tetra hydro furan). The further reaction of an aldehyde with Grignard reagent in the presence of
(d)
To determine: The accomplishment of given synthetic conversion.
Interpretation: The accomplishment of given synthetic conversion is to be stated.
Concept introduction: The conversion of a primary alcohol into aldehyde is done by PCC reagent. The further reaction of aldehyde with Grignard reagent in the presence of

Want to see the full answer?
Check out a sample textbook solution
Chapter 11 Solutions
Organic Chemistry (9th Edition)
- Part 1. Draw monomer units of the following products and draw their reaction mechanism (with arrow pushing) Temporary cross-linked polymer Using: 4% polyvinyl alcohol+ methyl red + 4% sodium boratearrow_forwardcan you please answer both these questions and draw the neccesaryarrow_forwardcan you please give the answer for both these pictures. thankyouarrow_forward
- Part 1. Draw monomer units of the following products and draw their reaction mechanism (with arrow pushing) | Bakelite like polymer Using: Resorcinol + NaOH + Formalinarrow_forwardQuestion 19 0/2 pts 3 Details You have a mixture of sodium chloride (NaCl) and potassium chloride (KCl) dissolved in water and want to separate out the Cl- ions by precipitating them out using silver ions (Ag+). The chemical equation for the net ionic reaction of NaCl and KCl with silver nitrate, AgNO3, is shown below. Ag+(aq) + Cl(aq) → AgCl(s) The total mass of the NaCl/KCl mixture is 1.299 g. Adding 50.42 mL of 0.381 M solution precipitates out all of the Cl-. What are the masses of NaCl and KCl in the mixture? Atomic masses: g: Mass of NaCl g: Mass of KCL Ag = 107.868 g mol- 1 Cl = 35.453 g mol- 1 K = 39.098 g mol- N = 14.007 g mol−1 Na = 22.99 g mol−1 0 = 15.999 g mol 1 Question Help: ✓ Message instructor Submit Questionarrow_forwardPart 1. Draw monomer units of the following products and draw their reaction mechanism (with arrow pushing) Polyester fiber Using a) pthalic anhydride + anhydrous sodium acetate + ethylene glycol B)pthalic anhydride + anhydrous sodium acetate + glycerolarrow_forward
- Identify the missing starting materials/ reagents/ products in the following reactions. Show the stereochemistry clearly in the structures, if any. If there is a major product, draw the structures of the major product with stereochemistry clearly indicated where applicable. Show only the diastereomers (you do not have to draw the pairs of enantiomers). If you believe that multiple products are formed in approximately equal amounts (hence neither is the major product), draw the structures of the products, and show the detailed mechanism of these reactions to justify the formation of the multiple products. If you believe no product is formed, explain why briefly. (6 mark for each, except f and g, which are 10 mark each)arrow_forward3. What starting material would you use to synthesize 3-hydroxypentanoic acid using a NaBH4 reduction?arrow_forward1. Give stereochemical (Fischer projection) formulas for all (but no extras) the stereoisomers that could theoretically form during the reduction of a. the carbonyl group of 2-methyl-3--pentanone b. both carbonyl groups of 2,4-pentanedione (careful!) 2. Predict the products of the reduction of O=CCH2CH2CH2C=O with a. LiAlH4 b. NaBH4 CH3 OHarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning


