4-ethyl-3-methyl 1 hexane
1) <u>Stereo-selective (or enantioselective)</u> reactions form predominately or exclusively one enantiomer.
2) Epoxidation is the addition of a single oxygen atom to an alkene to form an epoxide.
3) <u>Hydrogenation (or reduction)</u> of an alkene forms an alkane by addition of H₂.
4) <u>Dihydroxylation</u> is the addition of two hydroxy groups to a double forming, a 1,2-diol or glycol.
5) <u>oxidative</u> cleavage of an alkene breaks both the σ and π bonds of the double bond to form two carbonyl groups.
6) <u>Regioselective</u> reactions form predominately or exclusively one constitutional isomer.
7) <u>Syn</u> dihydroxylation results when an alkene is treated KMnO4 or OsO4, where each reagent adds two oxygen atoms to the same side of the double bond.
The atomic structure of the acetic acid is:
H O
l l
H –
C – C – O – H
l
H
We can see from the structure that there are 2 interior
atoms, and these are all Carbon atoms.
The geometry is:
Tetrahedral on First Carbon
Trigonal Planar on Second Carbon
Answer:
The correct answer is A. 140 atm
Explanation:
We use the gas formula, which results from the combination of the Boyle, Charles and Gay-Lussac laws. According to which at a constant mass, temperature, pressure and volume vary, keeping constant PV / T. We convert the unit Celsius into Kelvin:
0 ° C = 273K, 67 ° C = 273 + 67 = 340K; 94 ° C = 273 + 94 = 367K
P1xV1 /T1= P2x V2/T2
P2= ((P1xV1 /T1)xT2)/V2
P2=((88,89atm x 17L/340K)x367K)/12L= <em>135,927625 atm</em>
Answer:
By weight they have the same mass, but the number of atoms is different
Explanation: