Q: çI CH3 H3CHC=c-c-c=CH H H H3C 2) 3) CH3 H H H CI CH3 H3CHC-C-C=C-CH3 H
A: In a nomenclature first we have to find out the parent chain then we give numbers according to the…
Q: H H С—с—с—С—N -C- H. H H
A: FORMAL CHARGE RULE: Formal charge = No. of valance electrons - No. of non bonded…
Q: ОН О || CH3-CH-C-OH d. H2N-CH2-C-OH е. CH3 H3C. C-H ČH3 f.
A:
Q: CH-CH3 CH,CH, CH,CH3 CH CH,CH, H. H. H. CH3 -CH3 H. H. H. H' H. H H ČH3 IV H.
A: Answer- Conformarion in which both the bulkier group are at maximum distance or at opposite side…
Q: What is the configuration of each of the asymmetric centers in the following compounds?
A: Since you have posted a question with multiple sub-parts , we will solve first three parts for you.…
Q: CHy-C=C-H --> CHZCHZ CH3 a) CHS CH3 Oo --> b)
A: here we can make our desired product by first making halides of starting material by reacting one…
Q: С. Br d. -Ċ–CI CH, —CH—CH,—С—Вr CI е. f. g. CH;-C-F CH;-CH,-C–CI
A:
Q: N HN, CH2-C-NH2 CH2 O ters. H3N-C-C-N- CH-C-N- O=
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Q: + 2H2 H20 > B Na H3C-C: EC-CH3 + 1H2 A + Cl2 NH3(1) A H20 → B H2SO4 -c=c-CH3 + H2 Lindlar H,O H3C-C…
A: Hydrogenation is process of adding hydrogen across the unsaturated bond
Q: Are the following compounds primary, secondary, or tertiary?
A: a) The compound is tertiary, because the functional group bromine is attached to a tertiary carbon…
Q: Give the IUPAC name for each compound.
A: Aliphatic hydrocarbons are the linear chain compounds containing C and H. The nomenclature of these…
Q: Are the following pairs of structures resonance contributors or different compounds?
A: Hey, since there are multiple sub parts questions posted, we will answer first three questions. If…
Q: 1. CH3-C-CH3, CI-C-ċ-CI, -60°C (i) OH 2. (CH;CH2);N Na2Cr207 () -CH2-CH2-OH H2SO4
A:
Q: d. HC=C-CH(CH,CH,)CH,CH,CH, CH3 e. CH;CH2-C-C=CH ČH,CH,CH, f. CH,CH,C=CCHC=CCH3
A:
Q: CH3 CH3 CH C-C=CH CH3-CH,CC=CCH, CH3 IRE REI H3C H3CH2CC=CCH2CH3 H,C HCC CCH,CH3 ERI RIE Select one:…
A: Ozonolysis mechanism:
Q: CH2 но — с — сН,. CH N. CH HN H. z-I
A:
Q: CH3 CH from and H&C OCH,CH3
A: The given product can be synthesised from the reactants. Girgnard reagent is produced from alkyl…
Q: H H H H 2. H-C-C-C = C - H H H H
A: The given compound contains a carbon-carbon double bond, hence it is an alkene. The IUPAC name of an…
Q: CH3-CH2-OH Escrna) H Coy 0) 8. CHg-CH2-CH-CHgs EMPJHT
A: Since K2Cr2O7 and KMnO4 are strong oxidising agents. Hence primary alcohols on reaction with them…
Q: guur 39 t (s) II CH3-C-NH-CH3 A CH3-C-CI CH3-NH2 HCI II CH3-C-0-CH3 + H* B CH-С—он + CHз-ОН H20 OH…
A: Energy diagram
Q: HB Ha CH3 -CH3 C CH3 H D H3C A в HO
A: Given is structure of cholesterol. Let's draw chair form of it to check our answer.
Q: d. H3C KMNO4 ОН H3C е. OH CH3 KMNO, f. HI H3C-0–CH2 CH3
A:
Q: H3C, CI CH3 -СООН l\CH2OH CH2CH2NH ČH2OH HOH2C CH2CH2CH3 b. H3CH2C CI H,Clו H3C е. H3C OH d. 多I w |I
A: Rules to identify R and S Put the lowest priority substituent in the back (dashed line). Proceed…
Q: Ч Р 5 ____ Br I Н Cl — C — C — C —C —C = С | | CIH | | HCI Н Br HH Br H |||||||| |…
A: The IUPAC rules for naming the compounds are: 1. Select the longest chain of carbon. 2. Numbering…
Q: H₂CHN +2 CH3MgBr followed by H + CH3NH₂ B+ NaOH +CH₂I +CH₂OH. H* E +NaNO₂, HC1-F + CH3COCI G -D A с
A: We have to draw the product of following reaction given below:-
Q: но A Br2 в H2 D - CH,Br E Pd/C Answers A B D E molecular formul of E = C,H10
A: The missing reagents and the compounds for the given reaction can be given as: (A) Sulphuric acid…
Q: H H;CH,C NaCN Br acetone D Choose from the pool of choices below: H. CH3 H. CH3 H D. D H. АВС DEF H.…
A: Alkyl bromide most commonly undergoes addition and substitution reactions. Addition reactions are…
Q: What stereoisomers are obtained from each of the following reactions?
A: Since you have posted multiple sub-parts, we are entitled to answer the first three only.
Q: g. H3C NH3 H h. .N. i. H* H3C -C O-CH2CH3 H,0 エZ +
A:
Q: a) b) c) d) Br H ce CHz CNFCH-CH3
A:
Q: it-C-H HH # H H-C-C-C-C=C - C -C-H CH3 - CH- CH C-OH H H H-C-H H-C-H CH3 H-C-H O=U HICIH
A: Answer:- This question is answered by using the simple concept of writing the name of the organic…
Q: H. CH3 H. CH2CH3 H CH3 H. CH,CH3 H. H. CH3 H CH2CH3 H CH3 CH3
A: Projection 1 is the correct answer because when we see from C2 and C3 axis then it will form and…
Q: CI H,0 А (substitution) e) -CH3 H,0 B + C (elimination) major minor
A: A substitution reaction is a class of chemical reactions in which an atom, ion, or group of atoms…
Q: i. H* H3C-C-o-CH2CH3 H,0 j. H" о-н + H3C- HO- H3C
A: The given two reactions are hydrolysis of ester and esterification of carboxylic acid.
Q: CH3 f RR'CHОН + О-S `CH3 DCC, H* » ?
A: Dimethyl sulfoxide first attacks carboiimide which allows the added alcohol to attack positively…
Q: Explain why these two molecules are not isomers:
A:
Q: H. Br Br H H3C- FH OH CH3 Br Br F Br Br CH3 CH3 H- CI H- CI H- CI H- CH3 CH3 CH3 CH3 CI OH -H- CI H-…
A:
Q: For each of the reactions indicate which reactant is the nucleophile and which is the electrophile.
A: Since your question has multiple sub parts, we are solving only first three sub parts for you .If…
Q: Draw the products of the following reactions
A: Given reactions,
Q: CH,CH, CHg (b) CH, CH,CHg (c) HgC CH3 CH;CH,CHCH,CH,CHCH3 CH;CH-CH;CHCH>ÇCH3 CH3C-CCH,CH;CH3 CH3 HgC…
A: Please find the file attached for explanation
Q: H2C- CH3 H* ? + H;C- -C -CH3 H2C CH3 H2C-
A: When aldehyde or ketone react with diol in presence of acid it mostly forms cyclic acetal. This…
Q: -С-NCH-CH3 + HCI H2O H-0 a. ČH,CH3 1. CH3CH2MgBr 2. Нзо* b. CH;CH,ĊCH3 с. + (C,Hs)3P=CHCH3
A: Note: According to our guidelines we are supposed to answer only first three subpart.
Q: LIAIH4 (©) CH;CH;CH;I CH;CH,CH3 + - (d) H Ph H Ph C=C H;C-C-C-H H;C ОН ОН
A: Alkenes are compounds containing a double bond between carbon and carbon. The general molecular…
Q: Draw the products of the following reactions:
A: Since you have asked multiple question, we will solve the first question for you. If you want any…
Q: H-a Oi - :ö: + :CEN CN CH;-CH=CH, H-a CH3-ČH- CH2
A:
Q: Name the following:
A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…
Q: (a) CH3 (b) он (c) OH CH3CHCHCH2CH3 ČH,CH2CH3 HOCH2CH2ĊHCH2OH H. но (d) он (e) Ph. он (f) OH H CH3…
A: Note - Since you have posted a question with multiple sub-parts, we will solve the first three…
Q: А. B. C. D. HO w.. H3C CH3 CH₂ H CH3 CH3 CH3 CH3 HC3 CH3 HC3 CH3 Ž HC3 CH3 OH OH om CH3
A:
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- Sort the following according to whether they are monosaccharides, disaccharides, or polysaccharides. Drag the appropriate carbohydrates to their respective bins. • View Available Hint(s) Reset Help CH,OH HO H CH-O OH HO CH, CH,OH CH, OH ОН Н H CH-O H OH CH-O н но sucrose cellulose C-C H. ОН Н C Он Н H C-C CH H. OH Но C-C ÓH H Ć-Ć H ОН Н H OH H OH Monosaccharide Disaccharide Polysaccharide O.See attached image. Based on the results given above, which statement is most true? Sample A is a reducing sugar while Sample B is a nonreducing sugar. Sample A and Sample B are aldohexoses. Sample C is made up of a ketohexose and an aldohexose Sample A and Sample C are disaccharides while Sample B is a monosaccharide. Sample A, B, and C are all nonreducing sugars,Is this a pentose or octose? Thanks
- *22) Draw the Fischer projection and Hayworth formula for D-galactose - the C4 epimer of D- glucose. (Okay to skip this for discussion with molecular models in lab.) Fischer projection of D-galactose Hayworth formula of a-D-galactose Reactions and Disaccharides 23) Aldehydes are oxidized to: 24) Open-chain aldoses can be oxidized, so they are called 'reducing sugars'. When D-glucose is oxidized, what is the carboxylic acid formed? 25) Can the hemiacetal be oxidized? 25) Can a ketose be oxidized? CHM60 Lecture Worksheet: Carbohydrates J 5 2CH OH CH OH CH,OH CHOH CH2 CHOH O OH OH CH2 HO OH C 3 CHOH OH OH OH OH OH OH OH OH Download Image... The oligosaccharide was subjected to exhaustive methylation followed by acid hydrolysis. The product obtained for manosaccharide A is O A. 1,2,3,4,6-penta-0-methylfructose O B. 2,3,4-tri-O-methyfructose OC 1,3,4,6-tetra-O-methylfructose O D.2,3,4,5-tetra-O-methylfructose P Type here to searchBe sure to answer all parts. [1] classify the compound as a D or L monosaccharide; [2] draw the the enantiomer of the compound. [1] L [2] O draw structure... H H- OH -OH CH₂OH
- SC - Drawing the Haworth projection of a ketose from its Fischer projection Draw a Haworth projection of a common cyclic form of this monosaccharide: ! . . 1 HO HO H K Q CH₂OH C=O Explanation. A H -H OH CH₂OH N 2 W Click and drag to start drawing a structure- Check S #3 X E D $ 4 C R * F % 5 T 80 MacBook Pro A 6 G 7 V Y B & 287 7 H D 0 X * 0:0 U 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility * 00 8 5 J € - N M ( 9 K ✔ O ) 0 < L I' P - . 05 6 : { + 11 [ Le = ? I[Review Topics] A Fischer projection of a monosaccharide is shown below: CHO HO- H- H HO- -H -OH -OH -H CH₂OH Classify this monosaccharide (e.g., aldotriose) Does it have the D or L configuration? Submit Answer Retry Entire Group 9 more group attempts remaining [References] PreviDraw the Haworth projection of the disaccharide made by joining D-galactose and D-fructose with a B(1-4) glycosidic bond. If the disaccharide has more than one anomer, you can draw any of them. Explanation Check Click and drag to start drawing a structure. Q Search '0 X 3 FEET lo Ar © 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility
- Greenriverose is a fake disaccharide composed of \alpha -D-tagatose and \beta - D-allose (in that order) with a \alpha -2,2 glycosidic bond. build the full haworth structure of greenriverose with your model kit. DETAILEDQuest This molecule is a... CH₂OH + OH НО OH Opolucess OH O monosaccharide O disaccharide CH₂OH OH - OH OH НDraw the mechanism for the acid-catalyzed cyclization of D-fructose to give B-D-fructofuranose. Step 1 Draw curved arrows and lone pairs for step 1 of the mechanism. . .... H. II C HO 叫 O: FOH+ HO- -H- HO НО- H-OH H,O H- OH H- O- CI H- H- HO- Br 1. HO HO P. it I +it +t +l