Organic Chemistry Plus Mastering Chemistry with Pearson eText -- Access Card Package (9th Edition) (New in Organic Chemistry)
Question
Book Icon
Chapter 10.11B, Problem 10.26P

(a)

Interpretation Introduction

To determine: The synthesis of the given alcohol by reducing appropriate carbonyl compound.

Interpretation: The synthesis of the given alcohol by reducing appropriate carbonyl compound is to be shown.

Concept introduction: The synthesis of the primary or secondary alcohols is done by reaction carbonyl compound like carboxylic acid, ketone, aldehyde and ester by reducing agents like LiAlH4 or NaBH4 in the presence of appropriate solvent in the reaction.

LiAlH4 reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol. Sodium borohydride NaBH4 is a selective reducing reagent that reduces aldehyde to primary alcohol, and ketones to secondary alcohol.

(b)

Interpretation Introduction

To determine: The synthesis of the given alcohol by reducing appropriate carbonyl compound.

Interpretation: The synthesis of the given alcohol by reducing appropriate carbonyl compound is to be shown.

Concept introduction: The synthesis of the primary or secondary alcohols is done by reaction carbonyl compound like carboxylic acid, ketone, aldehyde and ester by reducing agents like LiAlH4 or NaBH4 in the presence of appropriate solvent in the reaction.

LiAlH4 reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol. Sodium borohydride NaBH4 is a selective reducing reagent that reduces aldehyde to primary alcohol, and ketones to secondary alcohol.

(c)

Interpretation Introduction

To determine: The synthesis of the given alcohol by reducing appropriate carbonyl compound.

Interpretation: The synthesis of the given alcohol by reducing appropriate carbonyl compound is to be shown.

Concept introduction: The synthesis of the primary or secondary alcohols is done by reaction carbonyl compound like carboxylic acid, ketone, aldehyde and ester by reducing agents like LiAlH4 or NaBH4 in the presence of appropriate solvent in the reaction.

LiAlH4 reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol. Sodium borohydride NaBH4 is a selective reducing reagent that reduces aldehyde to primary alcohol, and ketones to secondary alcohol.

(d)

Interpretation Introduction

To determine: The synthesis of the given alcohol by reducing appropriate carbonyl compound.

Interpretation: The synthesis of the given alcohol by reducing appropriate carbonyl compound is to be shown.

Concept introduction: The synthesis of the primary or secondary alcohols is done by reaction carbonyl compound like carboxylic acid, ketone, aldehyde and ester by reducing agents like LiAlH4 or NaBH4 in the presence of appropriate solvent in the reaction.

LiAlH4 reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol. Sodium borohydride NaBH4 is a selective reducing reagent that reduces aldehyde to primary alcohol, and ketones to secondary alcohol.

Blurred answer
Students have asked these similar questions
If I have 30% H2O2, indicate how to prepare a 6% H2O2 solution.
7) 8) FCI II -C-C-C=C-C || Br Br || -C=C-Br -CEC-C-C- 10) 11) F Br i OH مله 12) Br i 13) 14) 15) CH3CHFCHFC=CH C(OH)Br2CHF(CH2)4CH2CH3 CH3(CH2)3CH=CH(CH2)2CH3
Name 1) 3-fluoro, 1-butene 2) 2-heptene 2,3-difluoro- 1-pentene 4) 6-iodo,4-methyl- 2-decyne 5) 4,4-dibromo- 1,2-butandiol Complete structural formula F -C=C-C-C- Line formula Condensed structural formula N F CH2=CHCHFCH3

Chapter 10 Solutions

Organic Chemistry Plus Mastering Chemistry with Pearson eText -- Access Card Package (9th Edition) (New in Organic Chemistry)

Ch. 10.8B - Prob. 10.11PCh. 10.8B - Prob. 10.12PCh. 10.9A - Prob. 10.13PCh. 10.9B - Prob. 10.14PCh. 10.9C - Show how you would synthesize each tertiary...Ch. 10.9D - Prob. 10.16PCh. 10.9D - Show how you would add Grignard reagents to acid...Ch. 10.9D - A formate ester, such as ethyl formate, reacts...Ch. 10.9E - Prob. 10.19PCh. 10.9E - In Section9-7B, we saw how acetylide ions add to...Ch. 10.9F - Prob. 10.21PCh. 10.10A - Prob. 10.22PCh. 10.10B - Prob. 10.23PCh. 10.11B - Predict the products you would expect from the...Ch. 10.11B - Prob. 10.25PCh. 10.11B - Prob. 10.26PCh. 10.12 - Prob. 10.27PCh. 10.12 - Prob. 10.28PCh. 10.12 - Authentic skunk spray has become valuable for use...Ch. 10 - Give a systematic (IUPAC) name for each alcohol....Ch. 10 - Give systematic (IUPAC) names for the following...Ch. 10 - Draw the structures of the following compounds...Ch. 10 - Predict which member of each pair has the higher...Ch. 10 - Predict which member of each pair is more acidic,...Ch. 10 - Predict which member of each group is most soluble...Ch. 10 - Draw the organic products you would expect to...Ch. 10 - Prob. 10.37SPCh. 10 - Show how you would synthesize the following...Ch. 10 - Show how you would use Grignard syntheses to...Ch. 10 - Show how you would accomplish the following...Ch. 10 - Show how you would synthesize the following: a....Ch. 10 - Complete the following acid-base reactions. In...Ch. 10 - Prob. 10.43SPCh. 10 - Prob. 10.44SPCh. 10 - Geminal diols, or 1,1-diols, are usually unstable,...Ch. 10 - Vinyl alcohols are generally unstable, quickly...Ch. 10 - Compound A (C7H11Br) is treated with magnesium in...Ch. 10 - Prob. 10.48SPCh. 10 - Prob. 10.49SPCh. 10 - Prob. 10.50SPCh. 10 - Prob. 10.51SPCh. 10 - Prob. 10.52SPCh. 10 - Prob. 10.53SPCh. 10 - Prob. 10.54SPCh. 10 - Prob. 10.55SPCh. 10 - Prob. 10.56SPCh. 10 - Show how this 1 alcohol can be made from the...Ch. 10 - Prob. 10.58SPCh. 10 - Prob. 10.59SPCh. 10 - Prob. 10.60SP
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
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning