II). A. Draw a structure for each of the following compounds. 1. Styrene B 2- Ethoxybenzene 4. Acetophenone 3. Methanal OCH2CH3 HCHO 0 CH3 5. Phthalic Acid Name the following compounds (IUPAC or Common). COOH соон 1. . Cyclopentane carboxylic Adid 4. CH3CN 2. CH3COBr Acetyl Bromide Ethanoy! Bromide 5. Acetonitrile ur Cyanomethane NHCOCH3 Acetanilide OH COOH Salicylic Acid

II). A. Draw a structure for each of the following compounds. 1. Styrene B 2- Ethoxybenzene 4. Acetophenone 3. Methanal OCH2CH3 HCHO 0 CH3 5. Phthalic Acid Name the following compounds (IUPAC or Common). COOH соон 1. . Cyclopentane carboxylic Adid 4. CH3CN 2. CH3COBr Acetyl Bromide Ethanoy! Bromide 5. Acetonitrile ur Cyanomethane NHCOCH3 Acetanilide OH COOH Salicylic Acid

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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How many moles of Bra are required to completely halogenate the alkene?A. One moleB. Two molesC. Three molesD. Four moles What is the expected arrangement of the bromine atoms relative to each other amongthe carbon involved in pi bonding?A. anti-conformationB. syn-conformationC. trans-configurationD. cis-configuration What happens to bromine when it is adjacent to an alkene during a chemical reaction?A. Bromine becomes stable. (? kasi before brown siya/acidic tas naging colorless? Jk ewan)B. Bromine becomes polarized.C. Bromine becomes hybridized.D. Bromine becomes acidic. The relative arrangement of bromine atoms in the product is primarily due to:A. ElectronegativityB. RepulsionC. Hydrogen bondingD. Atomic weightWhat is your observation after the reaction?A. A yellow flame is produced.B. Bromine water decolorizes.C. The alkene becomes denser.D. A brown precipitate forms.
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1 Give an example (molecular structures) of each functional group. Use arbitrary alkyl groups (e.g., methyl, ethyl, etc.) ex. carbonate a b. C. d. e. f. 9. h. i. halohydrocarbons (for each halogen) alcohols (for primary, secondary, and tertiary) ethers aldehydes ketones carboxylic acids محمد esters amines (for primary, secondary, and tertiary) Draw the molecular structure of 4-chloro-2,5-dimethyl-3-heptanone. Draw the molecular structure of isopropyl acetate.
CH2 H3C H3C COOH Reagents e. PB13 f. NaCN then H3O* g. NBS, CCI4 h. CrO3, H2SO4 а. HBr b. Mg, ether c. CO2, ether then H3O* d. BH3, THF then H2O2, OH"
Reagents a. C6H5CHO b. NaOH, ethanol h. BrCH2CH=CH2 i. Na* OEt, ethanol j. Br2, H* k. K* t-BuO c. Pyrrolidine, cat. H* d. H2C=CHCN e. H3O* f. I. CH2(CO2ET)2 -CH2CH2CN LDA m. heat g. ELOC(=0)CO2ET Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda).
I. Name the following benzene derivatives in accordance to General Nomenclatures and IUPAC rules. NO2 NO2 CaHs Co ty 1. 4. CH-CH2 CH-CH NO cOcty CH2 NO2 NOz 5. NO cOcto I 3. 6. NH, 2. NO2 Authored by: Sensei Wilmark Palacios 7. 8. NH, cooH OH CAg 9. 10. COH I 2.
C. D. B. 1) Give the major organic product of the following reaction. Don't forget stereochemistry in certain cases. 2) Assign the reaction as addition, elimination, substitution, or rearrangement. A. D D 1. H₂O/Hg(OAC) 2 2. NaBH4 Br₂ CCl4 (inert solvent) H₂/Pd/C HBr Type of Reaction: Type of Reaction: Type of Reaction: Type of Reaction:
Structure please ?
9. Provide a systematic name for the following compound? A. 1,2,4-trimethyl-5-ethylcyclohexane B. 5-ethyl-1,2,4-trimethylcyclohexane C. 1-ethyl-2,4,5-trimethylcyclohexane D. 2,4,5-trimethyl-1-ethylcyclohexane 2 3
Draw the structures of the following hydrocarbon derivatives given in the screenshot. Please use either full structural diagrams or the combination method. Don't draw any Skeletal/line diagrams.
NOMENCLATURE, ANALYSIS & REACTIONS