C6H!0 has IHD = [6x2 +2-10] /2= 2
thus there can be two pi bonds or one pi bond and one ring.
However most acidic condition , makes it a terminal acetylene as CH of acetylene is acidic ( doublebonded or CH3 are not acidic)
optically active means , it must contain one chiral carbon at least with 4 different substituents.
thus the structure is
draw the most acidic, optically active constituional isomer or C6H10
orgonic chemistry
9A. An optically active compound (A), C6H10, reacts with H2,Pd/C to produce compound (B), C6H14. (B) is optically inactive. Identify (A) and (B). 9B. Why are vinylic halides unreactive in both Sn2 and Sn1 reactions?
Indicate whether the following substance is optically active or not.
optically active
optically inactive
cannot be determined
2. Draw the major product(s) formed when the optically active compound shown below is treated with H2O/H2SO4. Is the product optically active? Why or why not? (4 pts) optically active
3. Draw all the products, including all stereoisomers that form when the optically active compound below reacts with HCl. Which of these will be optically active? Mengh HCI optically active
Indicate whether the following substance is optically active or not. H|Ins optically active optically inactive O cannot be determined
Question 5: Draw the product(s) of this reaction (stereochemistry is important of products are optically active or not. + HBO
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers. The mixture had an observed specific rotation of 14.3°. If it is known that the specific rotation of the R enantiomer is –35.1°, determine the percentage of each isomer in the mixture.
is 3-methyl-1-pentyne a correct isomer for an alkyne with the
formula C6H10?
3-methyl-1-pentyne
1. Draw the MOST stable and the LEAST stable isomer of 3- chloro -4- methylhexane by drawing Newman Projections looking down the bond between Carbon -3 and Carbon-4 2. Circle the most acidic Hydrogen and then explain its acidity as needed with structures and sentençes NH2 OH
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers. The mixture had an observed specific rotation of +12.2°. If it is known that the specific rotation of the R enantiomer is - 36.5°, determine the percentage of each isomer in the mixture. Number R enantiomer: Number Senantiomer: