Which of the following structures is a skeletal structure for 1,2-difluoro-6- bromoheptane? Select one: Br a....
Question 5 Not yet answered Marked out of 1.0 P Flag question Which of the following compounds has the structure shown below? Select one: O a. 3-ethyl-5,6-difluoro-2-octanol O b. 3,4-difluoro-5-ethyl-7-octanol O C. 3-ethyl-5,6-difluoro-2-octanone O d. 3,4-difluoro-6-ethyl-7-octanal O e. None of the above Question 6 Not yet answered Marked out of 1.0 P Flag question What is the formula for the molecule shown below? Select one: O a. CisH27 NO O b. C16H38 NO O c. CisH26 NO O d. C16H26...
Question 4 Not yet answered Marked out of 1.0 Flag question Which of the following structures is a skeletal structure for 1,2-difluoro-6- bromoheptane? Select one: Br F. a. F Br Оъ. O c. Br F Br d. F enint Br е. L.
What are the names of the functional groups labelled 1,2 3? 3 Но. Select one: a. carboxylic acid, ketone, ether O b. aldehyde, alcohol, ketone c. aldehyde, ketone, ether d. alcohol, ether, ketone e. ketone, aldehyde, alcohol Which one is the correct organic product for the reaction shown below? он Select one: он a. b. C. ОН d. е. O
Which of the following compounds can have cis and trans isomers? 2-Methyl-2-butene Propene 0 1-Butene 1,2-Dichloro-1-Bu What is the correct molecular formula of 2,4-Diethyltouleno OCHA 0 C₂ H₂2 G H C:oH20 18 Which of the following compounds can have cis and trans isomers? 1-Butene 2-Methyl-2-butene 1,2-Dichloro-1-Butene Propene CH3CHBr2 is obtained from O Reaction of ethyne with one mole of HBr O Reaction of ethyne with one mole of Br2 Reaction of ethyne with two moles of Br2 Reaction of ethyne...
NBS Rxn Which one of the following is a major product of the reaction? Br Br NBS Heat Br Br -Br a b C ОА а O Bb O с с O D d Save Unanswered Acid/Base Equilibrium (FE) Which arrow best describes the acid/base reaction shown below? a IZ Oo b Oz + ОН с d O Аа O B b 0 CC O D d Save
QUESTION 1 For the following reaction, identify the 1,2-addition product. A) B) Br Br- Br + HBr C) D) Br ОООО С D 1 points QUESTION 2 Identify the product of the following reaction. + H,CO,C -CO,CH -CO,CH -CO_CH -CO,CH A CO,CH D) c) A) B) COACH CO,CH COCH, CO.CH B ОООО С D QUESTION 3 For (3E,5E)-octa-1,3,5,7-tetraene, shown below, how many of the a-molecular orbitals are bonding orbitals? 3 ОООО 6 PUS QUESTION 4 ОН ОН Which one of...
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...
* Question Completion Status: QUESTION 4 Is the following structure chiral? Ph. ČOOH Yes No QUESTION 5 1p Assign the correct stereochemical descriptor R or S according to the Cahn-Ingold-Prelog (CIP) nomenclature system to the following compound. Hint: The only possible answers are either the letters R or S- make sure to use CAPITAL letters, and only provide a single character. COOH NH2 н Me QUESTION z Is the following structure chiral? ОН НООС HO, O Yes O No QUESTION...
1-10 Name: Total 100 pts (25X4 pts) 1) Which of the following is the best name for the following compound? A) 1,2-Dichloropentanal )1-Chloro-1-butanecarbonyl chloride C) 2-Chloropentanoyl D) 1-Chloropentanoyl chloride 2) Which of the following is the best name for the following compound? 0 a) tsobutyl ethanoate d) Ethoxy isobutyl ketone b) Ethyl isopropanoate c) 3-methylbutyl ethanoate e) Ethyl 3-methylbutanoate 3) Which compound would have highest pKa? E) D) B) A) 4) Which of the following would be the strongest acid?...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...