2. Complete the structure below for the molecule (R)-2-bromobutan-1-ol. Br 3. Fill in the blanks in...
Fill in the blanks to complete the reaction. (3pts each) Br Н-С—с—н Mg CH3CHCH2CH3 1 Ether Br (CH),CО H 2 C CH-CH,ОH CH3CH20 + 3 E1OH CI 1. ВНз 2. NaOH, H02 ОН HO 5 (CH3CH2)2CuLi 6 OH Bi Br КОН 7 Нас NaCN DMSO
What is the IUPAC name of the molecule shown below HO Br Select one: O a. 7-bromo-2-cycloheptenol b. 1-bromo-3-cyclohepten-2-ol O c. 2-bromo-cycloheptenol O d. 2-bromo-6-cycloheptenol
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Indicate the stereo chemical configuration for the tetrahedral centers shown below. Select the proper IUPAC name for the following compound, including the (R) or (S) designation where appropriate. (R)-1-bromobutan-3-ol (S)-1 -bromobutan-3-ol (R)-4-bromobutan-2-ol (S)-4-bromobutan-2-ol Which carbon atom has the bromine attached, and what is the stereochemistry of that carbon? carbon-1 carbon- 2 carbon- 3 0rbon-4 Which carbon atom has the methyl group attached, and what is the stereochemistry of that carbon? carbon-1 carbon- 2 carbon- 3 carbon-4 R...
What is the IUPAC name of the given molecule? OH Br 1-bromo-2-ethyl-2-hydroxy-3-methylpentanoic acid 2-ethyl-3-methylpentan-2-ol-1-carboxyl bromide 2-ethyl-3-methyl-2-ol-pentanoyl bromide O2-ethyl-2-hydroxy-3-methylpentanoyl bromide What statement is TRUE about the mechanism for the reaction shown here? CH,(CH)2CO,CH, NaOH CH3(CH12COCH excess heat CH3(CH)2CO,CH2 Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is glycerol. The hydroxide deprotonates the alpha carbon. Which bases among the following is/are used...
Question 6 (4 points) What is the IUPAC name of the given molecule? Br OH 4-ethyl-5-ol-hexanoyl bromide 1-bromo-4-ethyl-5-hydroxyhexanoic acid 4-ethyl-5-hydroxyhexanoyl bromide 4-ethylhexan-5-ol-1-carboxyl bromide Question 7 (4 points) Predict the product for the following reaction: (CH3),Culi HO et
0/1 point Question 2 Expand the structure and name the compound Br H CH,CHE H3C сн. CH2(CH2),CH3 2-bromo-2-ethyloctane 1-bromo-3-ethylhexaneane 2-bromo-3-ethylcyclooctane 2-bromo-3-ethyloctane 0/ 1 point Question 4
3) Complete the reactions to show the multi-step syntheses of each product from (R)-2 bromo-3-methylbutane. Reaction conditions go in boxes above arrows (1 reaction/box) Complete the template molecules provided to show each step of the synthesis. [20] Hint- This question involves addition, elimination, substitution and alcohol chemistry Br (R)-2-bromo-3-methylbutane 3-methylbutan-1-ol (R)-2-bromo-3-methylbutane (R)-3-bromo-2 methylbutan-2-ol (R)-2-bromo-3-methylbutane (1-chloro-2-methylbutane (R)-2-bromo-3-methylbutane CN ()-1-cyano-3-methylbutan-1-ol
Name the following compound below with correct stereochemistry. CH Br r -H H-CH, CH,CH, (25,3S)-2-bromo-3-methylpentane (20,35)-2-bromo-3-methylpentane (25,3R)-2-bromo-3-methylpentane (2R 3R)-2-bromo-3-methylpentane
Question 31 Which is the IUPAC name for the structure shown below? Br A. (S)-5-Bromo-2-heptanal B. (R)-3-Bromopentyl methyl ketone C. (S)-5-Bromo-2-heptanone D. (R)-5-Bromo-2-heptanone E. (R)-5-Bromo-2-heptanal Question 32 Which structure represents an ester enolate? 09 I ΠΙ IV II A.1 B. II C. III D. IV E. Two of these choices.
If possible, draw the structure of the enantiomer of the molecule shown below. CH3 НАС Draw the enantiomer of the given molecule. If there is no enantiomer, draw the given molecule in the space provided. 2 . ⓇH1200 mm Marvin JS ChemAxon 1 oooooood