Using english to report chemistry ester
Ester Preparation Lab
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An ester is an organic compound which is created from a reaction between an acid and an alcohol, usually with the
loss of water. Many esters contain veer distinct odors, which has led
to them being used for artificial flavoring and fragrances. Esters can
be synthesized artificially in labs by combining alcohols and acids of
different strengths. This lab contained the synthesis of an ester by
allowing different carboxylic acids to react with alcohols, using
sulphuric acid as a catalyst, to create esters and allow the student to
identify them by their distinct smell. The smell was distinguished by
the different compounds that were created in the dehydration synthesis
reaction. Different safety techniques were taken into consideration to
ensure the lab was correctly executed. Special care was made while
handling the sulfuric acid due to its corrosiveness, while the special
‘wafting’ technique was used to detect the odors of the newly created
esters. To make sure the lab was done with the greatest amount of
safety, all participants wore eye protection, tied up any lose clothing,
tied long hair back and maintained a safe, well behaved manner.Purpose:
The purpose of this lab was to observe the synthesis of esters and identify the odor of each and then to write chemical equations of each ester synthesized.
| Chemical Name | Physical Properties | Potential Health Effects |
| Butanoic Acid | colorless liquid with a pungent, putrid odor. | No physical harming properties to humans, just small rodents |
| Salicylic Acid | White, odorless crystals | Contact with skin or eyes could lead to irritation, ingestion may cause nausea, headaches and dizziness |
| Malonic Acid | Fine white, odorless crystals | Causes both skin and eye irritation, Ingestion of sizable amounts can cause “salicylism”, as evidenced by abdominal pain, vomiting, increased respiration, and mental disturbances, irritation to skin and eyes if exposed |
| Ethanoic Acid | Colorless liquid, with strong vinegar like odor | Severe irritation, and burns to eyes and skin, breathing can irritate lungs |
| Propionic Acid | Clear oily liquid, slightly pungent irritating odor | Caues coughing and sneezing, ingestion leads to irritation and burns of digestive tract, causes severe skin and eye irritation and burns |
| Sulfuric acid (SO4/ H2SO4) | – Clear oily liquid – Odorless | – Poison
– Corrosive – Can cause severe burning to all body tissue – Inhalation produces damaging effects, including irritation of nose and throat and labored breathing – Ingestion can cause sever burns of the mouth, throat, stomach, leading to death – Skin contact has symptoms of redness and pain – Any eye contact and blur vision and cause blindness |
| Methanol (CH3OH) | -Clear, colorless liquid – Characteristic odor | – Poison
– Inhalation causes a slight irritation – Symptoms include headache, nausea, blindness, and death – Skin contact may cause skin to become dry and cracked – Irritant upon eye contact |
| Propanol CH3(CH2)2OH | – Clear, colorless liquid – Alcohol odor | – Symptoms include irritation of eyes, nose and throat and headache
– Ingestion can cause nausea, vomiting and drowsiness – Eye contact vapors are irritation to the eyes and may cause redness and tearing |
| 2-methyl-1-propanol (CH3)2CHCH2OH | – Clear, colorless solution – Sweet-musty odor | – Inhalation symptoms include headaches, dizziness and muscles weakness
– Ingestion may cause nausea, vomiting and diarrhea – Skin contact causes irritation, redness and pain – Eye contact cause irritation and blurred vision |
| Ethanol | -Colorless liquid – Agreeable odor | – Can irritate the skin
– Exposure can irritate the eyes, nose, mouth and throat – Breathing ethanol can irritate the lungs causing coughing and/or shortness of breath – Exposure can cause headache, nausea, a feeling of heat and drowsiness |
- Smell reactants before starting
- Label four test tubes A-D and place in test tube rack
- Into the appropriate test tube, using droppers, transfer an approximate amount of alcohol and carboxylic acid according to given table
- Add four drops of concentrated sulphuric acid into each test tube
- put 150 mL of water into a test tube and place the test tubes into the water, and heat the water on a hot plate to about 60 C, leave the test tubes un the hot bath for 15 minutes cool the test tubes by immersing in a cool water bath (second beaker)
- carefully note the odor
- using a dropper add 5 mL of distilled water in each test tube
- waft the test tubes again
- dispose of all materials following the reagent disposal instructions
Table 1
| Reactants | Odor |
| Butanoic Acid | |
| Methanol | |
| Ethanoic Acid | |
| 1-Propanol | |
| Salicylic Acid | |
| Propanoic Acid | |
| 2-Methyl-1-Propanol | |
| Maonic Acid | |
| Ethanol |
Products
| Odor (After cooled) | |
| Test Tube A | |
| Test Tube B | |
| Test Tube C | |
| Test Tube D |
| Products | Odor (After adding distilled water) | Appearance (after adding distlled water) |
| Test Tube A | ||
| Test Tube B | ||
| Test Tube C | ||
| Test Tube D |
what it is este and give me example r? thank you
BalasHapusEsters are organic chemical compounds whose structure has the general form:
Hapusgeneral molecular structure of an ester (class of organic compounds)
where the symbols "R1" and "R2" represent organic radicals, usually carbon chains.
[Symbols such as "R","R' ", "R1", "R2", "R1" and "R2" and similar are often used to represent organic radicals in general, which are frequently (linear or branched) carbon chains that may or may not have addtional functional groups attached, or can alternatively be hydrogen atoms or halogen atoms, e.g. flourine (F), chlorine (Cl), bromine (Br).]
In the case of esters, "R1" and "R2" are often carbon chains that may be either linear or branched and may also have other functional groups attached.
"R2" is not a hydrogen atom because if it were, the molecule would be a carboxylic acid rather than an ester.
The simplest esters to describe are those where both R1 and R2 are "an alkane less the hydrogen atom at the end of the chain", and hence where the hydrogen atom at the end of the corresponding alkane is replaced by the carbon or oxygen atom to which that "R" (so, R1 or R2 in the diagram above) is attached.
Why is the ester more volatile than alcohol? PLEASE EXPLAIN!!!!!!!!!
BalasHapusok iin,thnks fr ur question,,
HapusBecause ester properties are flammable and readily mixed with water and alcohol has a high boiling point compared to alkane acid. This is because the alcohol molecules contain lower -OH groups than the polar -OH groups. The chemical properties of the ester are based on a higher boiling point than the alcohol. And based on its structure it can be stated that carboxylic acid is a polar molecule. Carboxylic acid esters with relatively low molecular masses are generally colorless, car-colored and volatile and have odors. While the ester is a high molecular mass of liquid and volatile as well as small in the manufacture of ester reaction rates in the making
please explain, procedure about ester?
BalasHapusok,, procedure about ester
HapusSmell reactants before starting
Label four test tubes A-D and place in test tube rack
Into the appropriate test tube, using droppers, transfer an approximate amount of alcohol and carboxylic acid according to given table
Add four drops of concentrated sulphuric acid into each test tube
put 150 mL of water into a test tube and place the test tubes into the water, and heat the water on a hot plate to about 60 C, leave the test tubes un the hot bath for 15 minutes cool the test tubes by immersing in a cool water bath (second beaker)
carefully note the odor
using a dropper add 5 mL of distilled water in each test tube
waft the test tubes again
dispose of all materials following the reagent disposal instructions
So, what is the name of the ester synthesis reaction?
BalasHapusThe esterification process is a reversible reaction between a carboxylic acid and an alcohol. The esterified product is called an ester having a characteristic characteristic that is a fragrant smell. So it is generally used as a synthetic essence. The esterification reaction is a very slow reversible reaction. But when using a sulfuric acid or hydrochloric acid catalyst, the reaction equilibrium will be achieved within a few hours. Esterification is influenced by several factors such as; The molecular structure of the alcohol, the process temperature and the concentration of the catalyst as well as the reactants.
HapusEsters are derived from carboxylic acids by substituting OH groups with OR groups (R is an alkyl or aryl group). Esters are organic compounds that are neutral, not reacting with Na and PCl3 metals. Esters include one of the carboxylic acid derivatives obtained by reacting an acid (carboxylic) with an alcohol or phenol. The formula: RCOOR 'where R and R' are organic groups.
Can you give me the examples about the function of ester in the daily life?
BalasHapusESTER In everyday life we often consume a variety of fruit-flavored drinks that most probably do not really come from the original fruit but only diluted essens (fruit aroma). Essens are made of ester compounds whose aromas vary depending on the constituent ester
Hapustell me again Physical Properties of Malonic Acid?
BalasHapusFine white, odorless crystals
Hapus