Question
Book Icon
Chapter 9, Problem 60P

(a)

Interpretation Introduction

Interpretation:

The structure of products of given reaction should be drawn.

Concept Introduction:

Terminal alkynes are unusual for simple hydrocarbons in that they can be deprotonated using an appropriate base (typically  NaNH2 ) to generate a carbanion.

The acetylide carbanion is a good nucleophile and can undergo nucleophilic substitution reactions (usually SN2) with 1o or 2o alkyl halides (Cl, Br or I ) which have electrophilic to produce an internal alkyne.

3o alkyl halides are more likely to undergo elimination.

One or both of the terminal H atoms in ethylene HCCH can be substituted providing access to monosubstituted and symmetrical or unsymmetrical (R not equal to R') substituted alkynes RCCR' . The product is also an alkyne,

The SN2 reaction is a type of reaction mechanism in which one bond is broken and one bond is formed i.e., in one step. SN2 is a kind of nucleophilic substitution reaction mechanism.

(b)

Interpretation Introduction

Interpretation:

Two sets of reactants that could be used to synthesize a given compound should be given.

Concept Introduction:

Terminal alkynes are unusual for simple hydrocarbons in that they can be deprotonated using an appropriate base (typically  NaNH2 ) to generate a carbanion.

The acetylide carbanion is a good nucleophile and can undergo nucleophilic substitution reactions (usually SN2) with 1o or 2o alkyl halides (Cl, Br or I ) which have electrophilic to produce an internal alkyne.

3o alkyl halides are more likely to undergo elimination.

One or both of the terminal H atoms in ethylene HCCH can be substituted providing access to monosubstituted and symmetrical or unsymmetrical (R not equal to R') substituted alkynes RCCR' . The product is also an alkyne,

The SN2 reaction is a type of reaction mechanism in which one bond is broken and one bond is formed i.e., in one step. SN2 is a kind of nucleophilic substitution reaction mechanism.

(c)

Interpretation Introduction

Interpretation:

Two sets of reactants that could be used to synthesize a given compound should be given.

Concept Introduction:

Terminal alkynes are unusual for simple hydrocarbons in that they can be deprotonated using an appropriate base (typically  NaNH2 ) to generate a carbanion.

The acetylide carbanion is a good nucleophile and can undergo nucleophilic substitution reactions (usually SN2) with 1o or 2o alkyl halides (Cl, Br or I ) which have electrophilic to produce an internal alkyne.

3o alkyl halides are more likely to undergo elimination.

One or both of the terminal H atoms in ethylene HCCH can be substituted providing access to monosubstituted and symmetrical or unsymmetrical (R not equal to R') substituted alkynes RCCR' . The product is also an alkyne,

The SN2 reaction is a type of reaction mechanism in which one bond is broken and one bond is formed i.e., in one step. SN2 is a kind of nucleophilic substitution reaction mechanism.

Blurred answer
Students have asked these similar questions
Ch. 4- Precipitation Reactions Worksheet Write balanced, complete ionic, and net ionic equations for the following reactions that mav produce precipitates. Use NR to indicate no reaction Ave 1\ +3 =6 Fe + V-2 Na S04 13. Write the balanced equation for the reaction of iron (III) phosphate with sodium sulfate to make iron (III) sulfate and sodium phosphate. 2FePO4 + M, Soy a) If you perform this reaction with 25 grams of iron (III) phosphate and an excess of sodium sulfate, how many grams of iron (III) sulfate can you make? 21 Fe 2 3x 1 Na 3 25g Fe Ingle 150,829 Indes 2 nol 3 1335 349.89 35.90 Ihol & Sanz Fez Bak heck 3x1 50ab) If 18.5 grams of iron (III) sulfate are actually made when you do this reaction, what is your Poy percent yield? 118.5 259-1-100 51.4% (0.74)x100610 335 If you do this reaction with 15 grams of sodium sulfate and get a 65.0% yield, how many grams of sodium phosphate will you make? 10.59 14. Ammonia is produced from the reaction of nitrogen and hydrogen according…
== Functional Groups Identifying and drawing hemiacetals and acetals In the drawing area below, create an acetal with 1 isopropoxy group, 1 hydroxyl group, and a total of 10 carbon atoms. Explanation Click and drag to start drawing a structure. Check G +
State the products (formulas) of the reaction of acetophenone with iodine and NaOH.

Chapter 9 Solutions

Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)

Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning