Q1. Circle all functional groups (if any) and name them. Put the functional group of the...
H2N O. NH O NH2 НН nisin lanthipeptide 7) This partial structure is an antibacterial natural product called nisin isolated from Lactococcus lactis. Please find the following functional groups, circle one of them and write the corresponding letter next to the circled functional group A) Alcohol, B) Amine, C) Amide, D) Carboxylic Acid, E) Alkene, F) Heterocycle. Extra Credit: Circle and name an amino acid H2N O. NH O NH2 НН nisin lanthipeptide 7) This partial structure is an antibacterial...
1. Circle and name the functional groups in the compounds. (12 pts) amide OH NHCH, NH2 CH₃CHCH₂CH₂Coch, NO CH,CECCH_CHCH, 2. Name the compounds. (6 pts) CH₃ CH₂ CH,CHCH CHCH.CH -CH₂CH₂ b "CH₂CH₃
WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with the name of the group. NH OH COOH Alcohols | Chemistry 1113 87 WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with the name of the group. NH OH COOH Alcohols | Chemistry 1113 87
find and circle all the functional groups and name them CH3 Hac HN O NH CH H3C CH
1. In each molecule A-F below, circle and name two functional groups/moieties present in the molecule. Select from the list provided. [alcohol, ether, aldehyde, carboxylic acid, ester, amine, amide, propyl, alkyne, alkene - label as cis or trans when applicable, arene (for aromatic group)]. H2N- CH-OH CH2 HO H2CO | 0 NHA H2N IZ HO I- 0 m
H.C Macrocyclic lactone ring H₂C CH₂ Circle AND name four different functional groups in the compound to the right. CH to- HC-COM Io9 Hy 02 CHE You have an unknown containing five carbon atoms, has a pH of 6, yields a llow solution having no precipitate in a 2,4-DNP test, and produces a Jell-o like Dupreen solution in a chromic acid test. Name ONE functional group your unknown could contain You tested around 20 compounds containing 10 different functional groups...
C1) Name The Functional Group A X 5 HOL - Instance G 1. Compare and contrast the foll: X + nce.com/instances/9500#/experimentation/123282/exercise/48361 be some changes to the supplies in your kit. Please see the Student Help Center for information and instructions on affected items. Note: You will not draw the structure or build the molecular model of 1,2-dichloroethylpropanoate. Exercise 1 - Questions 1. Compare and contrast the following pairs of functional groups: a. Alcohols and ethers b. Aldehydes and ketones c....
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) он penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) СH3NH2 снзон HBr СHЗCH2CH2CH2СH3 HF
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) OH penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) HF CH3NH2 CH3OH HBr CH3CH2CH2CH2CH3
1. Identify all the functional groups in the following compounds. Circle each functional group and label each group. Thank you! 1. Identify all the functional groups in the following compounds. Circle each functional group and label each group. Hiç O CH CH CH-C-0-CHCH, -0-CH, CH CH(CH), a. acid group СОН) -CH-CHNHA 0-C-CH Amphetamine (a central nervous system stimulant and abused drug) O Aspirin ( 13 H1802 . . HC=CHCHACHACHCH CHO CHE e. HCCHI (CH OH CHE Citronellal alcohol group ~...