For any reducing sugar, there must be one free -OH group at anomeric position. The structure D does not contain any free -OH group at anomeric is non-reducing sugar and does not produce red solution on reaction with Tollen's reagent
Reducing Disaccharides Which of these would not give a red solution Сн,он with Tollens' reagent? сн,он -0. ОН СН2ОН...
Which or these would not give a red solution with Benedicts reagent? Reducing Disaccharides Which of these would not give a red solution CH2OH with Benedict's reagent? ÇH,OH (ОН CH,он HOV a-1,4-glycoside CH2OHN но то он ногоон А) он и Ион В-1,4-glycoside ОН Он он он В) CH2OH но —о а-1, В-1-glycoside CH2OH ул но —о. Ион он он/ a-1,6-glycoside но носн, он о HVOH YD) он ОН ОН он
Identify each of the disaccharides as a reducing sugar or a nonreducing sugar. Reducing sugar Nonreducing sugar CH, OH он CH OH CH OH OHN Кон ни и н IVO 5 5-т ен,он он н CH OH нон сн,он Сн,онн Үн нуконн Ин но он снон Кон вън онусн,он н он он н н Answer Bank
Testbank, Question 117 Which of the following disaccharides is a reducing sugar? ОН ОН ОН ОН но НОЈ HO ОН НО- ОН ОН НО но || он) OCH3 ОН Но То CH2OH ОН НО НО. он) СН2ОН о Но 7 CH2OH КОН CH2OH OH IV и он
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
Q1: CH, OH CHOH HO X OH OH OH a. Give common name of the given sugars. b. Name the glycoside linkage c. Identify them and reducing or non-reducing sugars d. Write the product for hydrolysis of these disaccharides Q 2: (a) Identify the type of isomers: СНО СНО но НО —н -н нон н — — ОН СН,ОН СН,ОН
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не — о он н ОН НА // Н v H ОН НА у н н н ОН н ОН CH,OH 1 ОНОН а снион и онон н СН,ОН ОН —0, ОН ОН ОН CH2OH -о- слъ We were unable to transcribe this imageQuestion 2 (1 point) Monosaccharide B can be cat Сн,ОН н Дон ү0 р. Н ОН HOCH2 ОН HV СН,ОН В. Г ОН...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair conformation of a-D-galactopyranose. 20. Which of the following compound(s) is a glycoside? 21. Provide the reagents neccesary to carry out the following conversion. 22. Predict the product(s) for the following reaction. 23. D-glucose & D-galactose are ______epimers of each other. 24. Predict the product(s) for the following reaction. 25. Which of the following compound(s) would produce D-glucose and D-mannose when treated with HCN followed...
Give the product(s) of reaction of hexanal with each of the following reagents. 2. (0) носн,сн,он, н (b) 1. LIAIH, 2. H,0* (e) NH,он, н" (d) NH,NH2, KOH, heat (e) (CH),СHCH,CH— P(C, Нә» , н" (g) Ag, NH, H,O (h) CrOs, H,SO H,0 () 1. KCN, 2. H,SO MCPBA Give the product(s) of reaction of hexanal with each of the following reagents. 2. (0) носн,сн,он, н (b) 1. LIAIH, 2. H,0* (e) NH,он, н" (d) NH,NH2, KOH, heat (e) (CH),СHCH,CH—...
organic chemistry 1.1 pt) Which reagent would you use to effect the following transformation of a diol into a keto acid? ОН Reagent? CH,CHCH,CH,CH,OH - CH,CCH,CH,сон a) Jones(H2Cr2O7) b) Tollens c) mCPBA d) Collins(PCC) e) LiAlH4 2.(2 pts) Circle the TWO compounds that yield a stable Grignard reagent when treated with magnesium in ether. Br CHÚC HỌC=CH- CH,OH HN 3.(2 pts each) Reactions. Complete each reaction shown here. HỌC=CH- + HC=CH- -CH OH он 1. CH CH MgBrCH,CH,CH=CHCCH2CH3 2.H2O Сн,...
Circle the one correct answer for our pluvieill. (100) A. The reaction of an alkene with chloroform (CHCl3) in the presence of a strong base, such as potassium tert-butoxide (KOC(CH3)3) gives a: a) epoxide b) aldehyde c) alcohold) cycloalkanee ) ketone B. Which of the following would give formaldehyde (H2C=0) upon treatment with aqueous periodic acid (HIO)? a) а) CH2OH b) d) н -он HO-LH CH OH CH OH Но HOH CH OH CH OCH3 Ε0 OH CH OH FO...