**Educational Content on Amines in Biologically Important Organic Compounds****Question:** Identify 1°, 2°, or 3° amines in the following biologically important organic compounds.1) **Structure 1:** - Chemical formula: \( \text{H}_2\text{N} - \text{CH}_2\text{CH}_2\text{CH}_2\text{CH}_2\text{CH}_2 - \text{NH}_2 \) - Compound Name: Cadaverine - Description: This structure represents a primary amine due to the presence of the amine group (-NH2) attached to a linear alkyl chain.2) **Structure 2:** - Functional Representation: A benzene ring with two hydroxyl groups (OH) and an ethylamine side chain. - Compound Name: Adrenaline (Nervous System Stimulant) - Description: Contains a secondary amine as the nitrogen atom is bonded to one hydrogen and two carbon atoms.3) **Structure 3:** - Functional Representation: A benzene ring with two hydroxyl groups (OH) and an amine (NH2) group directly attached. - Compound Name: Dopamine (Neurotransmitter) - Description: Displays a primary amine with the nitrogen atom bonded only to hydrogen and one carbon within the ring structure.4) **Structure 4:** - Functional Representation: A complex bicyclic structure with an ether (OCH3) and phenolic (OH) groups, along with a methylamine (N-CH3). - Compound Name: Codeine (Cough Suppressant) - Description: This is a tertiary amine, with the nitrogen atom bonded to three alkyl groups.**Reference:**- CHEL 114 – Session 11 – Lab Report Sheet- Authors: Khan, Raipara, Heidary- Date: 8/2020**Note:** In each compound, the amine degree is determined by the number of carbon-containing groups attached to the nitrogen atom. Primary (1°) amines have one, secondary (2°) have two, and tertiary (3°) have three such groups.

Amines are chemical compounds, in which nitrogen atoms are bonded with carbon atoms. On the basis of their attachments of N and C they are classified into primary (1°), secondary (2°), as well as tertiary (3°). On the following given structure, structure 3 and 1 of dopamine and cadaverine is primary amine because only one NH2 is attached to the one R group. Secondary amines are in which two R groups are attached to the one NH2. Hence, structure 2 is the secondary amine. The tertiary structure of amines is those, in which 3 R groups are associated with one amino group. Structure 4 is showing the tertiary amine.

Science

Biochemistry

Question: Identify 1°,2° or 3° amines in following biologically important organic compounds. 1) H2N-CH2CH2CH2CH2CH2NH2 (cadaverine) ОН H .N. "CH3 HO ОН 2) (Adrenaline-Nervous system stimulant) NH2 Но OH 3) (Dopamine - Neurotransmitter) CH,O. CN-CH, 4) HO (Codeine – Cough suppressant)

Question: Identify 1°,2° or 3° amines in following biologically important organic compounds. 1) H2N-CH2CH2CH2CH2CH2NH2 (cadaverine) ОН H .N. "CH3 HO ОН 2) (Adrenaline-Nervous system stimulant) NH2 Но OH 3) (Dopamine - Neurotransmitter) CH,O. CN-CH, 4) HO (Codeine – Cough suppressant)

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

Similar questions

5. Assign the IUPAC name for the following amines (15pts) C2H5 CH3-CH-CH-CH,-CH,CH2-CH2-CH3 a. b. CH3-CH2-CH2-NH-CH3 NH2
2. . questions below. Assume the following pKa values: N-terminal –NH3®, 7.0; all -COOH groups, 4.0; Arg, 12.5; Cys, 8.4; His, 6.0; Lys, 10.0; Tyr, 10.0. Calculate the overall charge (pH 7) on the following three polypeptides and answer the (A) Ser-Tyr-Ser-Met-Glu–His–Phe–Arg-Trp-Gly-Lys-Pro–Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys–Val-Tyr-Pro-Asp-Ala -Gly- Glu--Asp-Gln- Ser-Ala-Glu-Ala-Phe-Pro-Leu-Arg-Glu-Phe (B) Ser-Tyr-Ser-Met-Glu–His–Phe-Arg-Trp-Gly-Ala-Pro-Val-Gly-Glu-Glu-Cys-Asp-Pro-Val-Glu–Val-Tyr-Pro-Asp- Ala-Gly-Glu-Asp-Gln-Ser-Ala-Glu-Ala-Phe-Pro-Leu-Glu–Phe-Cys-Ser-Tyr-Ser-Met–Glu–His-Phe-Asp-Trp-Gly- Asp-Pro-Val-Gly-Pro-Asp-Ala-Gly-Asp-Gln-Pro-Val-Gly-Glu-Glu-Cys-Asp-Pro-Val-Glu-Val-Tyr-Pro-Asp-Ala (C) Gly-Ser-Val-Arg-Asp-Pro-Val-Lys-Glu-Val-Tyr-Pro-Asp- Lys-Ala-Gly-Arg-Glu-Ser-Arg-Ala (g) Which of the three peptides would migrate the furthest away from the anode in isoelectric fo- cusing (h) Which of the peptides would migrate the closest to the cathode in isoelectric focusing?…
Answer questions for the following monosaccharide: H-C-OH НО —с —н H C-OH d. Draw the product if it were oxidized ([O]). Draw entire product. H -C-OH e. Convert & draw the beta anomer (Haworth structure). CH2OH
ok-Personal Microsoft Edge com/maildeeplink 021 pdt Download Print Save to OneDrive 1. Draw the structure of the pentapeptide Gln-Trp-His-Glu-Tyr that would predominate in aqueous solution at pH3D10.3. (Relevant pka values are: 2.2 4.3, 6.0, 9.8, and 10.1) Acp is adiusted to
please answer (4)thanks !
I choose all the wrong ones can i get the corrections to the right answers please
please focus on this question 3 times i submitted it and three different answers, please make sure of ur answer
how to i draw this following lipid at PH 7.4. N-palmitoyl-D-erythro-sphingosylphosphorylcholine (aka16:0 sphingomyelin). thank you!
Please help with some explanation.
(please type answer no write by hand)