Connect 1-Semester Access Card for General, Organic, and Biochemistry
Connect 1-Semester Access Card for General, Organic, and Biochemistry
9th Edition
ISBN: 9781259815096
Author: Katherine J Denniston, Joseph J Topping, Dr Danae Quirk Dorr
Publisher: McGraw-Hill Education
bartleby

Concept explainers

Question
Book Icon
Chapter 16, Problem 16.64QP
Interpretation Introduction

Interpretation:

Reason for ketoses being oxidized in Benedict’s test while ketones are not oxidized has to be given.

Concept Introduction:

Benedict test is oxidation of aldehyde group present in aldoses.  The reagent used contains Cu2+ ions that is reduced to Cu+ ions when treated with aldoses.  A brick-red precipitate of Cu2O confirms the presence of aldehyde functional group.  Aldehyde group is oxidized to carboxylic acid.  If a hemiacetal hydroxyl group is present in the sugar then it will be a reducing sugar and the result will be positive for Benedict’s test.

Blurred answer
Students have asked these similar questions
For the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. 田 Major Product: Check ☐ + I Na OH esc F1 F2 2 1 @ 2 Q W tab A caps lock S #3 80 F3 69 4 σ F4 % 95 S Click and drag to sta drawing a structure mm Save For Later 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use GO DII F5 F6 F7 F8 F9 F10 6 CO 89 & 7 LU E R T Y U 8* 9 0 D F G H J K L Z X C V B N M 36
Problem 7 of 10 Draw the major product of this reaction. Ignore inorganic byproducts. S' S 1. BuLi 2. ethylene oxide (C2H4O) Select to Draw a Submit
Feedback (4/10) 30% Retry Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the reactant and missing intermediates involved in this reaction. Include all lone pairs and charges as appropriate. Ignore inorganic byproducts. Incorrect, 6 attempts remaining :0: Draw the Reactant H H3CO H- HIO: Ö-CH3 CH3OH2* protonation H. a H (+) H Ο CH3OH2 O: H3C protonation CH3OH deprotonation > CH3OH nucleophilic addition H. HO 0:0 Draw Intermediate a X

Chapter 16 Solutions

Connect 1-Semester Access Card for General, Organic, and Biochemistry

Ch. 16.3 - Prob. 16.8QCh. 16.4 - Prob. 16.4PPCh. 16.4 - Prob. 16.9QCh. 16.4 - Prob. 16.10QCh. 16.4 - Prob. 16.5PPCh. 16.6 - Prob. 16.11QCh. 16.6 - Prob. 16.12QCh. 16 - Prob. 16.13QPCh. 16 - Prob. 16.14QPCh. 16 - Prob. 16.15QPCh. 16 - Prob. 16.16QPCh. 16 - Prob. 16.17QPCh. 16 - Prob. 16.18QPCh. 16 - Prob. 16.19QPCh. 16 - Prob. 16.20QPCh. 16 - Prob. 16.21QPCh. 16 - Prob. 16.22QPCh. 16 - Prob. 16.23QPCh. 16 - Prob. 16.24QPCh. 16 - Prob. 16.25QPCh. 16 - Prob. 16.26QPCh. 16 - Prob. 16.27QPCh. 16 - Prob. 16.28QPCh. 16 - Prob. 16.29QPCh. 16 - Prob. 16.30QPCh. 16 - Prob. 16.31QPCh. 16 - Prob. 16.32QPCh. 16 - Prob. 16.33QPCh. 16 - Prob. 16.34QPCh. 16 - Prob. 16.35QPCh. 16 - Prob. 16.36QPCh. 16 - Prob. 16.37QPCh. 16 - Prob. 16.38QPCh. 16 - Prob. 16.39QPCh. 16 - Prob. 16.40QPCh. 16 - Prob. 16.41QPCh. 16 - Prob. 16.42QPCh. 16 - Prob. 16.43QPCh. 16 - Prob. 16.44QPCh. 16 - Prob. 16.45QPCh. 16 - Prob. 16.46QPCh. 16 - Prob. 16.47QPCh. 16 - Prob. 16.48QPCh. 16 - Prob. 16.49QPCh. 16 - Prob. 16.50QPCh. 16 - Prob. 16.51QPCh. 16 - Prob. 16.52QPCh. 16 - Prob. 16.53QPCh. 16 - Prob. 16.54QPCh. 16 - Prob. 16.55QPCh. 16 - Prob. 16.56QPCh. 16 - Prob. 16.57QPCh. 16 - Prob. 16.58QPCh. 16 - Prob. 16.59QPCh. 16 - Prob. 16.60QPCh. 16 - Prob. 16.61QPCh. 16 - Prob. 16.62QPCh. 16 - Prob. 16.63QPCh. 16 - Prob. 16.64QPCh. 16 - Prob. 16.65QPCh. 16 - Prob. 16.66QPCh. 16 - Prob. 16.67QPCh. 16 - Prob. 16.68QPCh. 16 - Prob. 16.69QPCh. 16 - Prob. 16.70QPCh. 16 - Prob. 16.71QPCh. 16 - Prob. 16.72QPCh. 16 - Prob. 16.73QPCh. 16 - Prob. 16.74QPCh. 16 - Prob. 16.75QPCh. 16 - Prob. 16.76QPCh. 16 - Prob. 16.77QPCh. 16 - Prob. 16.78QPCh. 16 - Prob. 16.79QPCh. 16 - Prob. 16.80QPCh. 16 - Prob. 16.81QPCh. 16 - Prob. 16.82QPCh. 16 - Prob. 16.83QPCh. 16 - Prob. 16.84QPCh. 16 - Prob. 16.85QPCh. 16 - How does the structure of amylose differ from that...Ch. 16 - Prob. 16.87QPCh. 16 - Prob. 16.88QPCh. 16 - Prob. 16.89QPCh. 16 - Prob. 16.90QPCh. 16 - Prob. 1CPCh. 16 - Prob. 2CPCh. 16 - Prob. 3CPCh. 16 - Prob. 4CPCh. 16 - Prob. 5CPCh. 16 - Prob. 6CP
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY