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- Question 4 of 4 O Macmillan Learning Organic Chemistry Maxwell Classify the mechanism as a substitution, elimination, or addition reaction. >/. CI The mechanism is: elimination addition substitution + O -H presented by Macmillan Learning + H₂O + CI:2 mehgiheene ..syclohexene. HO H. P-benzoicacid.2 SUPERMARKET23 4 Essay Writing Ser. G calculator - Googl. A Gflights b BATERBLY C CHEGG > KATAPULK CUBA O Maps a AMAZON A Translate Question 6 of 21 Which of the following best describes why only small aldehydes and ketones are soluble in water? A) low molar mass aldehydes and ketones can hydrogen bond through the carbonyl oxygen to water. B) High molar mass aldehydes and ketones have boiling points that are too high to be soluble in water. C) low molar mass aldehydes and ketones hydrogen bond with one another to be soluble in water. D) low molar mass aldehydes and ketones have low boiling points that enhance solubility in water. MacBook Pro 23 2 3 4 7 8 W E R Y F G H. J K T
- 7) You want to synthesize 3-methyl-2-pentene from 2-chloro-3-methylpentane. Which reagent would you use? a. HCI, heat b. NH:(aq), 25°C c. CH:CO2NA, CH:CO2H, heat d. CH3CH2ONA, CH3CH2OH, heat e. CН:CH2ОН, heatPlease explain how it forms an alkene? I am the problems and my CH3s keep aligning like in question "a", when they should be anti to each other? Please explain how they are suppose to form? Thank youComplete the following reactions? 1). NaBH¾/ethanol ii). H3O* H. i). LIAIH,/ether ii). H3O*
- 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.1. Analyze the related pair of words/phrases associated with phenols. Vanillin: oxidation of eugenol; Ortho-quinone: _____________ Isopropyl: Propofol; _____________: BHT Benzene: cyclohexatriene; _____________: cyclohexadienedionefull structural form is needed for complete reaction h.w
- Each H↔H eclipsing interaction in ethane costs about 4.0 kJ/mol. How many such interactions are percent in cyclopropane? What fraction of the overall 115 kJ/mol (27.5 kcal/mol) strain energy of cyclopropane is due to torsional strain.Give IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para (p), no italics, if you elect to use these terms. CH₂CH₂CHCHCHSCHCH₂ I T CH₁ CH₂ 1st structure: CH3 CH3 I 2nd structure: Submit Submit Answer Try Another Version OCH3 CH₂CCH₂ OCH3 10 item attempts remainingBe sure to answer all parts. Draw the structure corresponding to each IUPAC name. a. 6-ethyl-2-octyne I I 1 I -CH₂ I I H₂C edit structure... b. 5,6-dimethyl-2-heptyne I I I I I draw structure...
