Answer:
Enantiomers/ Isomers/ Stereoisomers/ Meso compounds/ Constitutional isomers/ Diastereomers.
Explanation:
Isomers are molecules that have the same chemical formula but have different conformation, or in its connections, or the orientation in space. Isomers have different chemical and physical properties (second blank).
The isomers that only differ by the orientation of their atoms in space are called stereoisomers (third blank).
The stereoisomers that have a chiral carbon and do not mirror images of each are called enantiomers (first blank). They can deviate the polarized light.
When a compound has two or more chiral carbons but they compensate for the deviation of the light, and the compound is optically inactive, it's called a meso compound (fourth blank).
When the isomers differ in the way the atoms are connected it's called a constitutional isomer (fifth blank).
When the molecule has more than one chiral carbon, it will have pairs of enantiomers. The isomers that aren't of the same pair are nonsuperimposable mirror images of each other and are called diastereomers (last blank).
According to the question, the determined melting point of the compound is 112.5-113.0oC. When the solidified compound was retried, the melting point was found to be 133.6-154.5oC. This greater range higher than 112°C is caused by reusing samples leads to errors.
A pure sample is known by its sharp melting point. A pure sample does not melt over a large range. We can see this in the predetermined melting points of the pure sample(112.5-113.0oC).
However, reusing a sample introduces errors because the pure sample may become contaminated leading to a larger and higher range of melting point (133.6-154.5oC) which is far above 112°C.
Learn more: brainly.com/question/5325004
Answer:
Explanation:
The polarity of the 3 compounds would be in the order of
Ferrocene < Acetylferrocene < Diacetylferrocene
Your TLC data has to also support this observation . This can be checked by measuring the values of Rf ( Retention factor = distance travelled by solute/solvent ) .The Rf values also has to follow this particular order: -
Ferrocene > acetylferrocene > diacetylferrocene
2) Hexane happens to be a non-polar solvent. The polarity of hexane can be increased if some polar solvents for example, ethyl and methylene chloride etc are added
Therefore, in the increasing order of solvents polarity, we have
Hexane < 1:1 mixture of hexane: methylene chloride < 9:1 mixture of methylene chloride:
3) Chromatographic techniques all have a stationary phase in addition to a mobile phase. In the case of column chromatography, the silica gel will be the stationary phase and the solvent that will be poured will be the mobile phase.
4) The TLC and column chromatography both happen to have the same stationary phase which is the silica gel. Also, the same solvent mixture is used in both the techniques. This makes the result of the 2 to be almost the same. The difference seen between them is that, TLC works against the gravity while on the other hand column chromatography works in the direction of the gravity.
5) The key feature in the IR spectra of the acetylferrocene that will be absent in the spectra of ferrocene is the presence of carbonyl stretching frequency at close to 1700 per cm(cm-1). This peak is easily differentiated between both acetyl ferrocene and ferrocene.
<span>H2PCH3 + H2O <-----> H3PCH3+ + OH-</span>
Answer:
Explanation:
Concentration: i is defined as the mole per litre.
mole=0.15
volume=400 ml=0.4 litre
