C) Draw all of the different meso-products that can form from B) above. In order to be different they must have different names.
A)
Vicinal dibromide is produced when bromine molecule adds to C=C
double bond of an alkene in cold and dark.
A vicinal dibromide has 2 bromine atoms on adjacent C atoms.
A geminal dibromide has 2 bromine atoms on same C atom.
A vicinal bromohydrin has a bromine atom and a hydroxyl group on
adjacent C atoms.
B)
trans-3-hexene gives meso products.
The remaining gives racemic mixture.
1-hexene gives prodcut containing only chiral C atom. The product is a racemic mixture.
C)
Only one meso product is possible.
C) Draw all of the different meso-products that can form from B) above. In order to...
Look up and draw the mechanism for the addition of Br2 to
double bonds. Reference the source from which you acquired the
mechanism.
Give the IUPAC name of the major product in the above-mentioned
reaction.
Draw the major product of obtained in the addition of Br2 to
stilbene.
Is this isomer chiral? What would be the optical rotation if
this sample was placed in a polarimeter?
Would a student obtain the same product if you started with
cis-stilbene instead of...
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon chain. b.Find the longest carbon chain containing the alkene. c. Find whether the alkene has a cis- or trans- configuration. d.Find how far the alkene functionality is from either end. 2. What is the IUPAC name of the following alkene? a. cis-5-methyl-2-heptene b. trans-2-ethyl-4-hexene c. trans-5-methyl-2-heptene d. trans-3-methyl-5-heptene 3. What is the hybridization, geometry, and bond angle of the carbon marked by an asterisk?...
Postlab Questions Answer the following questions on a separate sheet or in your lab notebook. Make sure that the copy page is readable! D) Calculate the percentage yield for both reactions. Show all calculations. 2) What is the color of the reaction at the beginning of reaction? What causes the color? 3) Why do you dissolve maleic acid in diethyl ether and fumaric acid in water? 4) Give the complete reaction mechanisms for the formation of meso and racemic 2,3-...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...
26) Name the following compound. CH3 H2C=CH-CH2CHCH: A) 1,1-dimethyl-3-butane B) 4-methyl-1-pentene C) hexene D) 2-methyl-4-pentene E) 2-methylpentene 27) Name the following compound. CI A) 2,3,5-trichlorobenzene B) trichlorostyrene C) 1,3,4-trichlorobenzene D) 1,3,4-trichlorohexene E) 1,2,4-trichlorobenzene 28) Identify the formula for an alkene. A) CnH2n+4 B) CnH2n+2 C) CnH2n D) CnH2n-4 E) CnH2n-2 29) Name the following compound. A) 1,4-bromocyclohexene B) 1,4-dibromobenzene C) 3,6-dibromobenzene D) 2,5-dibromobenzene E) 2,5-dibromocyclohexene 30) Name the following compound. CECH CH,CH,CHCH A) 2-ethynebutane B) 3-methyl-1-pentyne C) 3-methyl-4-pentyne D) 3-ethyl-1-butyne...
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...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....