1) Label the acidic functional groups
2) For each acidic site, indicate if it has been drawn in the protonated form or not
1) Label the acidic functional groups 2) For each acidic site, indicate if it has been...
1. Match each structure to the functional group a alcohol b. aldehyde c. ketone d. acid e. esterf. amine HC CH, OH ii. iii. ОН iv. OH H vi. NH2 vii. 2. For each of the following, write the formula (abbreviated) a. OH b. ОН c. 2. What is stereospecificity? Why is it important? 3. For each molecule below, identify the functional groups. НО а. Сн,он СН,ОН ОНИ ОН b. ОН ОН Н.N. О НО. о с.. ОД d. но...
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
Page 2 of 2 Quiz 5- CHM130 4. Determine the functional groups in each of the following compounds H2C он CH3 H3C н.с H3C H3C Lovastatin Aspirin Lipitor CH но CH3 CH3 Capsaicin NH HN CH но н.co ,o он HO H но Vitamin C он он Chlorophyll core Salicylic acid
Page 2 of 2 Quiz 5- CHM130 4. Determine the functional groups in each of the following compounds H2C он CH3 H3C н.с H3C H3C Lovastatin Aspirin Lipitor CH...
Which carbonyl group in the molecule below is the least
reactive?
How many functional groups undergo hydrolysis to a carboxylic
acid in the molecule shown?
не ор N. ОН a о НО A A B с с D E E 0 HN- NC LO -N 0 A Two B Three с Four D Five E Six
Name the functional groups for Carbon 1 and Carbon 6
on both structures.
С— н 1 6 CH2OH Н. -ОН н -о он Он но- H -н 1 ndieoue n он -ОН H H Он -ОН 6 CH-он I
eferences Find and name all of the functional groups in each of the following. (Select all that apply.) (a) Glycocholate OHHC сну . NH CH2 COOH н,С HO ОН alcohol carbon-carbon double bond ester aldehyde carbon-carbon triple bond ether amide carboxylate anion ketone amine carboxylic acid thiol
1. For the molecule below a) Circle and label all functional groups. b) Name all intermolecular forces present in the molecule: Amane Aromates hetone lendon dspervon Dipale -Dipole Amine Aromatr 2. For the molecule below a) Box in all atoms that can hydrogen bond with water but not with acetone (CH3OCHS) b) Label all electrophilic carbons (use 6*) NH c) Label the least basic nitrogen. НО d) Label the most acidic hydrogen
1. Circle and name the functional groups in the following molecules a) capsaicin Но осон нс. е. т н I- IÓ н н 0 CH H3o C G CH3 O= DI O b)-Arachidonoyl dopamine HO c) porphyrin CH3 CH3 CH3 CH3 H,C- CH3
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 ~...
uestion 2 Rank these molecules in order of decreasing acidity [that is, most acidic first.] 1. CHCHCO2Н 2. CH-CHCO,н F 3. CH-CН-СО,Н 2 3 1 2> 1> 3 1> 2 3 3> 2 11 O 1>3> 2 Question 3 Which compound is the most acidic? Cl CI C Question 5 Which of the following molecules is the product of an aldol reaction? ОН HO HO IV ОН and IV Question 11 Which of the following contains an amide functional group?...