Examples of 'reaction yield' in a sentence
Meaning of "reaction yield"
reaction yield: This term is used in chemistry to describe the amount of product obtained from a chemical reaction, typically in relation to the amount that could theoretically be produced
How to use "reaction yield" in a sentence
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reaction yield
The reaction yield is practically quantitative.
An excess of histidine was used to facilitate the reaction yield.
Marked improvement in the reaction yield and conversion is observed.
The reaction yield is therefore limited by the presence of water.
The amount of product in a chemical synthesis is the reaction yield.
Low reaction yield also leads to increase of a production cost.
The aim of this modification is to increase the reaction yield.
Amidation reaction yield.
The reaction yield is high as is the purity of the reaction products.
This process is preferred because the reaction yield is high.
This means that the reaction yield is not reduced by these unwanted regioisomers.
This increase in reactivity also determines a significant increase in the reaction yield.
Such additive increases the reaction yield by suppression of side reactions.
By applying a temperature outside these ranges would decrease the reaction yield.
The polymer is weighed and the reaction yield and catalyst activity is calculated.
See also
The amount of base selected may affect the overall reaction yield.
The reaction yield is measured and confirmed by using a known method such as gas chromatography.
The presence of water in the reaction medium has an influence on the reaction yield.
The reaction temperature lowers the reaction yield when it is too high or too low.
Reaction Yield of.
In fact, high temperatures reduced the reaction yield.
An increased reaction yield and a large increase in MIBK productivity are thus observed.
On the other hand, additional oxygen is required to achieve a higher reaction yield.
Moreover, the reaction yield was found to be low.
However, when the temperature is higher, side reaction occurs to decrease the reaction yield.
The reaction yield and results obtained are given in table 3.
As indicated before, the etherification reaction yield is determined by the water content.
The reaction yield and physicochemical characteristics of this compound are given in table 1.
If the difference is too large, the reaction yield tends to decrease, such being undesirable.
Such energetic conditions generate a significant amount of by-products that consequently diminish the reaction yield.
Furthermore, the reaction yield is reduced due to a parasitic secondary reaction.
Furthermore, the addition of oxygen improves the reaction yield for numerous catalytic systems.
As a result, a reaction yield or purity of the target product is not increased.
The present invention relates to a process for producing vanadium-arenes, with a high reaction yield.
In addition, the reaction yield is reduced as a result of a parasitic or competing secondary reaction.
Further, there still remains a room for improvement also with respect to the reaction yield.
Moreover, the reaction yield is not satisfactory due to the formation of by-products.
PH is adjusted to 3 when the reaction yield is optimal.
Besides, the reaction yield of a penem antibiotic intermediate may be also improved.
Samples were taken and analysed on a SE-HPLC column to determine the reaction yield.
Second column reflects reaction yield after ( x ) recrystallizations of enantiomer after initial separation.
This retrogradation affects the purity of the UDETA, and also the reaction yield.
The reaction yield is 66 % with respect to the pivalaldehyde introduced.
The organic solution is titrated with HPLC thus obtaining a molar reaction yield of 34 %.
The reaction yield is,.
The physicochemical characteristics of this compound and the reaction yield are given in table 1 . EXAMPLE 7.
The reaction yield with respect to the quantity of anhydrous starch used was 90 %.
When it is less than 5 %, the reaction yield is less increased.
The reaction yield is 48 % and the product obtained is analyzed by nuclear magnetic resonance.
At the end of the synthesis, the reaction yield is checked to be about 95 %.
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