Answered: Identify the circled functional groups…

Identify the circled functional groups and linkages in the compound below. OH CH3 H-N+c+CH2CH2-N-C+c c–CH2 B CH," H H CH2 0-P=0 (SH 0-P=0 D CH2 0 ОН H H H H 203PO E F

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

See similar textbooks

Related questions

Q: Name the following compound. CH;-NH A) ethyl amine B) dimethyl ether C) methanal D) 1-methanoate E)…

A: Amine is an organic compound and it has a nitrogen atom attached to hydrogen and an alkyl group…

Q: What is glycoside? Classify the glycosides depending on the atom involved in glycosidic bond…

A: There are a lot of natural organic compounds that are present in plants and some animals. These can…

Q: Identify the functional group designated by RCOOH, alkane O carboxylic acid ester O alcohol o…

A: In organic chemistry, functional groups are a group of atoms or moieties which constitute the…

Q: Order the following from polar to nonpolar. Acetone Nitromethane

A: A condition or state of a molecule or an atom consisting of negative and also positive charges,…

Q: Indicate whether each of the following statement about enantiomers is True or False. a. Enantiomers…

A: Spatial isomerism or stereoisomerism is a type of isomerism in which the molecules have the same…

Q: Draw the structure and give the name of the epimers of the following monosaccharides ALDOTRIOSE I…

Q: Draw a structural formula for each compound. (a) trans-2-Methyl-3-hexene (b) 2-Methyl-3-hexyne (c)…

A: Structural formula for each compound are given in the next step,

Q: Draw skeletal structure for the following structures: a. (25, 3R)-dichloropentane b. (25, 3R, 4R)-2…

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: Classify the following as an Alcohol, Phenol, Thiol, Ether, Aldehyde or Ketone. ОН CH HÇ HC CH CH OA…

A: Organic compounds are the chemical compounds that deals with the bonding of one or more carbon atom…

Q: Study the given structures below. Which of the following are enantiomers?" -OH но- H- HO- но- HO-…

A: Enantiomers are molecules that are exact mirror images of each other. They cannot be superimposed on…

Q: (e) (f)

A: IUPAC name of the given figure e) and f),

Q: CH,OH CH,OH OH H OH H OH OH H H OH OH H

A: Sugars are polyhydroxy alcohols. Polysaccharides are the polymers of monosaccharides attached…

Q: All of the following have terpene structure, except Cholecalciferol Squalene Carotenoids O…

A: Terpenes are hydrocarbons composed of 5 carbon atoms attached to 8 hydrogen atoms. Terpenes consists…

Q: 1. Cirde and identify three different functional groups on the following diagram OH 1. 2. 3.

A: Functional groups are the unique arrangement of atoms in a molecule. They impart distinctive…

Q: Galactose can exist as a cyclic hemiacetal because one of the alcohol groups reacts with the…

A: Galactose is defined as the monosaccharide sugar that is a stereoisomer of glucose. It can exist as…

Q: 1. 2. 3. 4. 5. Name n-Pentane (CsH12) Chloroethene (C₂H3C1) Bromoethyne (C₂HBr) Ethanol (C₂H6O)…

A: Lewis structure is a method of representing the structure of a chemical compound by using a valence…

Q: ldentify the Fischer projection A to D that matches each of the following: (15.1, 15.3) the L…

A: Fisher projection is used to depict three-dimensional compounds into two-dimensional. Enantiomers or…

Q: Name the following compound. CH,-OH A) 3-pentanol B) 2-ethyl-1-butanol C) 3-methyl-3-pentanol D)…

A: in this OH must be in the main chain so chain starts from OH. and from this, on the 2nd carbon…

Q: Write the systematic (IUPAC) names for the amines. The names should have the format alkanamine.…

A: Amines are the class of chemical compounds having alkyl or aryl groups attached to the nitrogen…

Q: Following are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses.…

A: Chiral molecules can exist in the configurations that are non-superimposable mirror images of each…

Q: Write the IUPAC name for each unsaturated hydrocarbon. (a) CH,=CH(CH2),CH3 CH3 H,C- (b) CH3 CH3 (c)…

A: IUPAC names for each unsaturated hydrocarbon given in the 2nd step,

Q: VII. Identify the functional groups present. No need to name the compounds. H нн нн H H…

A: Functional groups: These are the atoms or group of atoms attached with the chemical compounds and…

Q: Refer to the figure below.The functional groups shown are the group,the group, and the group C…

A: All living organisms are made up of cells, which are the most basic unit of life. They are…

Q: Draw the structures of the following acids:(a) 2-Ethyl-3-hydroxyhexanoic acid (b) m-Nitrobenzoic…

A: Acids are those chemical compounds, which are known to lose (H+) protons in the solution.

Q: Provide compounds that fit the following descriptions:(a) Two amines that are gases at room…

A: Amino acids are organic compounds that combine to form proteins. They are the building blocks of…

Q: The name of compound in the following image according to IUPAC nomenclature is

A: The given question deals with the naming of an organic compound based on IUPAC system of…

Q: Classify the alcohol with the following structure: NHCOCH, CH,OH Select one: a. none of the other…

A: Step 1 The carbon next to the carbon with which the alcohol is attached determines whether it is…

Q: Arrange the following FAs in decreasing melting point. * A. A 22-carbon series saturated FA B. An…

A: Melting point of Fatty acids depend upon several factors like Molecular weight Degree of Saturation…

Q: Which of the following is the cyclic form of an L saccharide? 1) II) CH2OH OH H CH2OH H H H OH H ÓH…

A: The preferred form of monosaccharides is a cyclic hemiacetal. 5 or 6 membered rings because of their…

Q: Write chemical names for the following compounds: (a) Thymidine (b) Cytosine (c) Uracil (d) Xanthine…

A: Chemical names are names written based on their chemical composition, which make up that compound.…

Q: Give the systematic name of the the disaccharide shown below: CH2OH -O, H CH2OH H Н ОН Н OH Н ОН Н H…

A: This carbohydrate is a disaccharide that is composed of two monosaccharides. Two monosaccharides are…

Q: H3C- -CH3 CH3 H3C CH3 Но ČH3 -CH3 A B D H2N NH2 OH CH3 -CH3 -CH3 H3C- CH3 H3C- H3C CH3 H;C ČH3 F G H

A: A functional group is a substituent in a molecule which governs it's characteristics of chemical…

Q: H HN-C-C-OH H-C-CH, CH2 CH3 The following short passage is about the compound with chemical…

A: Protein is a polymer formed from amino acid joined by peptide bond. There are twenty standard amino…

Q: ÕH CONH, 0= NH (CH3)3C 1. a.) Put asterisk on chiral centers b.) label each chiral center as R or S.…

A: The chiral centers are the atoms which are bonded to four different groups through single bond such…

Q: Leterofunctional compounds Name the following compound: 0 HOOC-C-CH,COOH

A: Heterofunctional compound : An organic substances that contain two or more different functional…

Q: The chemical structure of ethane (C2H6) is provided below. Which of the following isomers is ethane…

A: Option (5) none of the above is correct answer. (1) Ethane only have one form. It has too few…

Q: Identify the Lewis acid in the following reaction: A. BF3 B. F C. BF4 D. None of these is an acid.…

A: Boron trifluoride (BF3) is a Lewis acid because it is an electron-deficient molecule that may take…

Q: Draw structures corresponding to the following names:(a) 2,4-Dimethylheptan-2-ol(b)…

A: Introduction –Alcohols are the organic compounds in which it contains one or more than one hydroxyl…

Q: J. ach compound on the left with its name on the right. Match the name with the functional E. group…

A: Functional groups are atoms that bind to an organic molecule's carbon backbone and give certain…

Q: 4. -C-O-C- A compound that contains the above alcohol alkoxy group antioxidant dehydration reaction…

A: Biological molecules are composed of different functional groups which include hydroxyl, methyl,…

Q: Draw a Lewis structure for hydroxylamine, NH2OH.

A: Lewis structure is also known as Lewis dot structure, which represents lines for the bonding between…

Q: Please draw all four bonds at chiral centers. Use wedge and dash bonds at chiral centers only. Do…

A: Enantiomers are the compounds that are mirror image to each other but are not superimposable .

Q: Draw structures corresponding to the following names:(a) 3-Methylhexan-1-ol (b)…

A: Alcohol is the class of the organic compound that has attached OH group with the alkyl carbon in its…

Q: The molecules shown below are: CH HN HN CH2 H. OH H OH OH O A= deoxyadenylate; B = thymidylate A=…

A: DNA consists of three types of component: phosphate, a sugar called deoxyribose, and four…

Q: Answer the following:

A: Functional group: It is a group of atoms with different chemical properties than the other atoms in…

Q: Write the IUPAC name for the following compounds? Br (a)

A: IUPAC or International Union of Pure and Applied Chemistry has devised some some rules in naming…

Question

For A, B, C, D, E, F, identify the circled functional groups and linkages in the compound in the picture.

. dentify the circled functional groups and linkages in the compound below.
ОН СНз
H-NC+CH2CH2-N-C+ç-c-CH2
В
CH2
O H H
CH2
0-P=0
(SH
A
-0-P=0
D
CH2 O
ОН
H
H
н
(20;PO
OH
E
F

Definition Definition Group of atoms that shape the chemical characteristics of a molecule. The behavior of a functional group is uniform in undergoing comparable chemical reactions, regardless of the other constituents of the molecule. Functional groups aid in the classification and anticipation of reactivity of organic molecules.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step 3

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 steps

SEE SOLUTION Check out a sample Q&A here

Similar questions

Following are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers. CHO сно H-C- OH H-C-OH H-C- OH но-с — н н-с—он но- ČHOH ČH,OH сно CHO Н-с—он но—с— н H-C- OH H-C-OH но—с—н Н-с—он ČHOH ČH,OH сно сно н-с—он но—с —н но—с— н но -с — н H-C- OH но- C-H ČH,OH ČH,OH
Based on the following titration table of Glycine, would you be able to recreate the same for Histidine? Glicina Increasing pH H-N-CH,-COOH -H-N-CH,-co = H-N-CH,-C00- Net charge: +1 pH COOH-pKa = 2.3 NH3-pka = 9.6 CN AEq +1 +1 2.3 (0.5°-1)+(0.5°0)=-0.5 +0.5 0.5 9.6 -1 (0.5*+1)+(0.5°0)=+0.5 -0.5 1.5 14 Given that the pKas for Histidine are the following: pka1 = 1.82 pKa2 = 9.17 pКаз %3 6.00 pL = 7.59 2.
Consider the structure of the tripeptide (in its fully protonated form) below. H H H + I || H₂N-C-C-N-C-C-N-C-C-OH 1 I | H CH₂ H CH₂ CH₂ T C=O OH AA1 0=0 || HC-CH3 CH3 AA2 AA3 0=C 1. Give the sequence of the tripeptide using the ONE-LETTER DESIGNATION (UPPERCASE LETTER) with NO spaces and symbols between each letter. 2. How many ionizable groups are there in the tripeptide? Give the numerical value (e.g., 10 not ten). • pH 10: {Choices: -2, -1, 0, +1, +2} 3. Which amino acid residue has one ionizable group left upon forming the tripeptide? {Choices: AA1, AA2, AA3, none, all} 4. Give the net charge of the dominant structure of the tripeptide at the given pH values. The pK, values of the amino acids are given in Table 1. • pH 4: {Choices: -2, -1, 0, +1, +2}
Write the name for the trisaccharide depicted below (for example, of the form a - D - xylofuranose). Be sure to include if the sugars are in the pyranose or furanose conformations in the name and include the linkages between sugars (for example, (2 - - > 4)). CH₂OH ОН OH н ОН -CH₂ H\H ОН н н ОН CH2OH н ОН но н н ОН
Consider the structure of the tripeptide below. H O 11 H₂N-C-C-N-C-c- CH₂ CH₂ C=0 NH₂ pH 5: Z-I pH 10: H HN H O 11 CH₂ NH HIC- I-Z 0=6 -N-C-C-OH 1. What is the sequence of the tripeptide? (use the one-letter symbol, do not put dash or space in between symbols) 2. What is the net charge of the dominant structure of the tripeptide at the given pH values? The pK, values of the amino acids are given in Table 1. CH-OH T CH3 Table 1. pk, values of the standard amino acids.
Based on the following titration table of Glycine, would you be able to recreate the same for Histidine? Increasing pH – Glicina H H-N-CH,-COOH = H-N-CH,-CO0- = H-N-CH,-coo- H H Net charge: +1 -1 pH COOH-pKa = 2.3 NH3-pKa = 9.6 CN ΔΕ +1 +1 2.3 (0.5*-1)+(0.5*0)=-0.5 +1 +0.5 0.5 9.6 -1 (0.5*+1)+(0.5*0)=+0.5 -0.5 1.5 14 -1 -1 2 Given that the pKas for Histidine are the following: pka1 = 1.82 pKa2 = 9.17 pКа3 %3D 6.00 pl = 7.59
Look at the structure of the disaccharide shown. Name the type of bond which is present. CH,OH H H он но CH2 Он H он H ÓH O B - 1, 4- N-glycosidic linkage O a- 1, 4- O-glycosidic linkage O B- 1, 4-0-glycosidic linkage O a- 1, 6- 0-glycosidic linkage O a- 1, 4- N-glycosidic linkage
In the following scheme: HH, H₂C-C-C-Coo II HO H • NH, 1 H₂C-C-C-C000 H 2-Amino-3-ketobutyrate ↓ O H,C-C-CH₂-NH₂ Aminoacetone 0 0 H₂C-C-C-H Methylglyoxal H H₂C-C-COO OH D-Lactate O H₂C-C-C000 Pyruvate What molecule is being metabolized? Identify the reaction at each step. If it is an oxidation-reduction prove this is correct by showing oxidation state changes on the atoms in the structure.
In the space provided, draw a Haworth projection for the beta anomer of the following monosaccharide Fischer projection. CHO HO-C-H HO-C-H HO-C-H H-C-OH CH,OH
Determine the number of possible stereoisomers for the fol- lowing compounds: CH,OH C=0 CH,OH Но-с—н C=0 H-C-OH H-C-OH H-C-OH H-C-OH H-C-OH CH,OH CH,OH Ribulose Sedoheptulose
Draw one aromatic polar amino acid at pH 7. Label with full name, three letter abbreviation, and single letter symbol.
Which of the following is the correct systematic name of the disaccharide shown? OH он но но но- OH Он a-D-glucopyranosyl-(1-3)-B-D-galactopyranose O a-D-glucopyranosyl-(1–3)-B-D-glucopyranose O a-D-gulopyranosyl-(1-4)-B-D-glucopyranose O a-D-gulopyranosyl-(1-4)-B-D-galactopyranose