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20.3 Aldehydes, ketones, carboxylic acids, and esters  (Page 3/9)

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Formaldehyde, an aldehyde with the formula HCHO, is a colorless gas with a pungent and irritating odor. It is sold in an aqueous solution called formalin, which contains about 37% formaldehyde by weight. Formaldehyde causes coagulation of proteins, so it kills bacteria (and any other living organism) and stops many of the biological processes that cause tissue to decay. Thus, formaldehyde is used for preserving tissue specimens and embalming bodies. It is also used to sterilize soil or other materials. Formaldehyde is used in the manufacture of Bakelite, a hard plastic having high chemical and electrical resistance.

Dimethyl ketone, CH 3 COCH 3 , commonly called acetone, is the simplest ketone. It is made commercially by fermenting corn or molasses, or by oxidation of 2-propanol. Acetone is a colorless liquid. Among its many uses are as a solvent for lacquer (including fingernail polish), cellulose acetate, cellulose nitrate, acetylene, plastics, and varnishes; as a paint and varnish remover; and as a solvent in the manufacture of pharmaceuticals and chemicals.

Carboxylic acids and esters

The odor of vinegar is caused by the presence of acetic acid, a carboxylic acid, in the vinegar. The odor of ripe bananas and many other fruits is due to the presence of esters, compounds that can be prepared by the reaction of a carboxylic acid with an alcohol. Because esters do not have hydrogen bonds between molecules, they have lower vapor pressures than the alcohols and carboxylic acids from which they are derived (see [link] ).

There are nine structures represented in this figure. The first is labeled, “raspberry,” and, “iso-butyl formate.” It shows an H atom with a line going up and to the right which then goes down and to the right. It goes up and to the right again and down and to the right and up and to the right. At the first peak is a double bond to an O atom. At the first trough is an O atom. At the second trough, there is a line going straight down. The second is labeled, “apple,” and, “butyl acetate.” There is a line that goes up and to the right, down and to the right, up and to the right, and down and to the right. At the second peak is a double bond to an O atom. At the end, on the right is O C H subscript 3. The third is labeled, “pineapple,” and, “ethyl butyrate.” It is a line that goes up and to the right, down and to the right, up and to the right, down and to the right, up and to the right, and down and to the right. At the second peak is a double bond to an O atom and at the second trough is an O atom. The fourth is labeled, “rum,” and “propyl isobutyrate.” It shows a line that goes down and to the right, up and to the right, down and to the right, up and to the right, down and to the right and up and to the right. The first complete peak has a double bond to an O atom and the second trough has an O atom. The fifth is labeled, “peach,” and “benzyl acetate.” It shows a line that goes up and to the right, down and to the right, up and to the right and down and to the right. This line connects to a hexagon with a circle inside it. The first peak has a double bond to an O atom and the first trough has an O atom. The sixth is labeled, “orange,” and, “octyl acetate.” It shows a line that goes up and to the right and down and to the right and up and to the right and down and to the right and up and to the right and down and to the right and up and to the right and down and to the right and up and to the right and down and to the right. The first peak has a double bond to an O atom and the first complete trough has and an O atom. The seventh is labeled, “wintergreen,” and “methyl salicylate.” It shows a hexagon with a circle inside of it. On the right, is a bond down and to the right to an O H group. On the right is a bond to a line that goes up and to the right and down and two the right and up and to the right. At the first peak is a double bond to an O atom, the next trough shows and O atom and at the end of the line is a C H subscript 3 group. The eighth is labeled, “honey,” and “methyl phenylacetate.” It shows a hexagon with a circle inside of it. It shows it connecting to a line on the right that goes down and to the right then up and to the right and down and to the right and up and to the right. At the first peak that is not part of the hexagon is a double bond to an O atom. At the last trough is an O atom. The ninth is labeled, “strawberry,” and “ethyl methylphenylglycidate.” This shows a hexagon with a circle inside of it. On the right, it connects to a line that goes up and to the right and down and to the right and up and to the right and down and to the right and up and to the right and down and to the right. At the first peak is a line that extends above and below. Below, it connects to an O atom. At the next trough, the line extends down and to the left to the same O atom. At the next peak is a double bond to an O atom and at the next trough is an O atom.
Esters are responsible for the odors associated with various plants and their fruits.

Both carboxylic acids and esters contain a carbonyl group with a second oxygen atom bonded to the carbon atom in the carbonyl group by a single bond. In a carboxylic acid, the second oxygen atom also bonds to a hydrogen atom. In an ester, the second oxygen atom bonds to another carbon atom. The names for carboxylic acids and esters include prefixes that denote the lengths of the carbon chains in the molecules and are derived following nomenclature rules similar to those for inorganic acids and salts (see these examples):

Two structures are shown. The first structure is labeled, “ethanoic acid,” and, “acetic acid.” This structure indicates a C atom to which H atoms are bonded above, below and to the left. To the right of this in red is a bonded group comprised of a C atom to which an O atom is double bonded above. To the right of the red C atom, an O atom is bonded which has an H atom bonded to its right. Both O atoms have two sets of electron dots. The second structure is labeled, “methyl ethanoate,” and, “methyl acetate.” This structure indicates a C atom to which H atoms are bonded above, below and to the left. In red, bonded to the right is a C atom with a double bonded O atom above and a single bonded O atom to the right. To the right of this last O atom in black is another C atom to which H atoms are bonded above, below and to the right. Both O atoms have two pairs of electron dots.

The functional groups for an acid and for an ester are shown in red in these formulas.

The hydrogen atom in the functional group of a carboxylic acid will react with a base to form an ionic salt:

A chemical reaction is shown. On the left, a structure of propionic acid is indicated. This structure includes a 2 carbon hydrocarbon group on the left end in black. Above, below, and to the left, H atoms are bonded. This group is bonded to a red group comprised of a C atom to which an O atom is double bonded above. To the right of the red C atom, an O atom is connected with a single bond. To the right of the O atom, an H atom is bonded. To the right of this structure appears a plus and N a O H. Following the reaction arrow, the propionate ion is shown. This structure is in brackets. Appearing inside the brackets, is a 2 carbon hydrocarbon group on the left end. Above, below, and to the left, H atoms are bonded. To the right of this group, a group in red is attached comprised of a C atom to which an O atom is double bonded above and a second O atom is single bonded to the right. Outside the brackets appears a superscript minus symbol. This is followed by a plus sign, N a superscript plus another plus sign and H subscript 2 O. The singly bonded O atom in the propionate ion structure has 3 pairs of electron dots. All other O atoms have two pairs of electron dots.

Carboxylic acids are weak acids (see the chapter on acids and bases), meaning they are not 100% ionized in water. Generally only about 1% of the molecules of a carboxylic acid dissolved in water are ionized at any given time. The remaining molecules are undissociated in solution.

We prepare carboxylic acids by the oxidation of aldehydes or alcohols whose –OH functional group is located on the carbon atom at the end of the chain of carbon atoms in the alcohol:

A chemical reaction with two arrows is shown. On the left, an alcohol, indicated with a C atom to which an R group is bonded to the left, H atoms are bonded above and below, and in red, a single bonded O atom with an H atom bonded to the right is shown. Following the first reaction arrow, an aldehyde is shown. This structure is represented with an R group bonded to a red C atom to which an H atom is bonded above and to the right, and an O atom is double bonded below and to the right. Appearing to the right of the second arrow, is a carboxylic acid comprised of an R group bonded to a C atom to which, in red, an O atom is single bonded with an H atom bonded to its right side. A red O is double bonded below and to the right. All O atoms have two pairs of electron dots.

Esters are produced by the reaction of acids with alcohols. For example, the ester ethyl acetate, CH 3 CO 2 CH 2 CH 3 , is formed when acetic acid reacts with ethanol:

A chemical reaction is shown. On the left, a C H subscript 3 group bonded to a red C atom. The C atom forms a double bond with an O atom which is also in red. The C atom is also bonded to an O atom which is bonded to an H atom, also in red. A plus sign is shown, which is followed by H O C H subscript 2 C H subscript 3. The H O group is in red. Following a reaction arrow, a C H subscript 3 group is shown which is bonded to a red C atom with a double bonded O atom and a single bonded O. To the right of this single bonded O atom, a C H subscript 2 C H subscript 3 group is attached and shown in black. This structure is followed by a plus sign and H subscript 2 O. The O atoms in the first structure on the left and the structure following the reaction arrow have two pairs of electron dots.

The simplest carboxylic acid is formic acid, HCO 2 H, known since 1670. Its name comes from the Latin word formicus , which means “ant”; it was first isolated by the distillation of red ants. It is partially responsible for the pain and irritation of ant and wasp stings, and is responsible for a characteristic odor of ants that can be sometimes detected in their nests.

Questions & Answers

Three charges q_{1}=+3\mu C, q_{2}=+6\mu C and q_{3}=+8\mu C are located at (2,0)m (0,0)m and (0,3) coordinates respectively. Find the magnitude and direction acted upon q_{2} by the two other charges.Draw the correct graphical illustration of the problem above showing the direction of all forces.
Kate Reply
To solve this problem, we need to first find the net force acting on charge q_{2}. The magnitude of the force exerted by q_{1} on q_{2} is given by F=\frac{kq_{1}q_{2}}{r^{2}} where k is the Coulomb constant, q_{1} and q_{2} are the charges of the particles, and r is the distance between them.
Muhammed
What is the direction and net electric force on q_{1}= 5µC located at (0,4)r due to charges q_{2}=7mu located at (0,0)m and q_{3}=3\mu C located at (4,0)m?
Kate Reply
what is the change in momentum of a body?
Eunice Reply
what is a capacitor?
Raymond Reply
Capacitor is a separation of opposite charges using an insulator of very small dimension between them. Capacitor is used for allowing an AC (alternating current) to pass while a DC (direct current) is blocked.
Gautam
A motor travelling at 72km/m on sighting a stop sign applying the breaks such that under constant deaccelerate in the meters of 50 metres what is the magnitude of the accelerate
Maria Reply
please solve
Sharon
8m/s²
Aishat
What is Thermodynamics
Muordit
velocity can be 72 km/h in question. 72 km/h=20 m/s, v^2=2.a.x , 20^2=2.a.50, a=4 m/s^2.
Mehmet
A boat travels due east at a speed of 40meter per seconds across a river flowing due south at 30meter per seconds. what is the resultant speed of the boat
Saheed Reply
50 m/s due south east
Someone
which has a higher temperature, 1cup of boiling water or 1teapot of boiling water which can transfer more heat 1cup of boiling water or 1 teapot of boiling water explain your . answer
Ramon Reply
I believe temperature being an intensive property does not change for any amount of boiling water whereas heat being an extensive property changes with amount/size of the system.
Someone
Scratch that
Someone
temperature for any amount of water to boil at ntp is 100⁰C (it is a state function and and intensive property) and it depends both will give same amount of heat because the surface available for heat transfer is greater in case of the kettle as well as the heat stored in it but if you talk.....
Someone
about the amount of heat stored in the system then in that case since the mass of water in the kettle is greater so more energy is required to raise the temperature b/c more molecules of water are present in the kettle
Someone
definitely of physics
Haryormhidey Reply
how many start and codon
Esrael Reply
what is field
Felix Reply
physics, biology and chemistry this is my Field
ALIYU
field is a region of space under the influence of some physical properties
Collete
what is ogarnic chemistry
WISDOM Reply
determine the slope giving that 3y+ 2x-14=0
WISDOM
Another formula for Acceleration
Belty Reply
a=v/t. a=f/m a
IHUMA
innocent
Adah
pratica A on solution of hydro chloric acid,B is a solution containing 0.5000 mole ofsodium chlorid per dm³,put A in the burret and titrate 20.00 or 25.00cm³ portion of B using melting orange as the indicator. record the deside of your burret tabulate the burret reading and calculate the average volume of acid used?
Nassze Reply
how do lnternal energy measures
Esrael
Two bodies attract each other electrically. Do they both have to be charged? Answer the same question if the bodies repel one another.
JALLAH Reply
No. According to Isac Newtons law. this two bodies maybe you and the wall beside you. Attracting depends on the mass och each body and distance between them.
Dlovan
Are you really asking if two bodies have to be charged to be influenced by Coulombs Law?
Robert
like charges repel while unlike charges atttact
Raymond
What is specific heat capacity
Destiny Reply
Specific heat capacity is a measure of the amount of energy required to raise the temperature of a substance by one degree Celsius (or Kelvin). It is measured in Joules per kilogram per degree Celsius (J/kg°C).
AI-Robot
specific heat capacity is the amount of energy needed to raise the temperature of a substance by one degree Celsius or kelvin
ROKEEB
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Source:  OpenStax, Chemistry. OpenStax CNX. May 20, 2015 Download for free at http://legacy.cnx.org/content/col11760/1.9
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