Thermodynamic quantity equivalent to the total heat content of a system It is equal to the internal energy of the system plus the product of pressure and volume
Answer:
The answer is E. All of the statements describe the anomeric carbon.
Explanation:
When a sugar switches from its open form to its ring form, the carbon from the carbonyl (aldehyde if it is an aldose, or a ketone in the case of a ketose) suffers a nucleophilic addition by one of the hydroxyls in the chain, preferably one that will form a 5 or 6 membered ring after the reaction.
As such, the anomeric carbon will have two oxygens attached (The original one and the one that bonded when the ring closed).
It will be chiral, given that it has 4 different groups attached. (-OR,-OH,-H and -R, where R is the carbon chain).
The hydroxyl group can be in any position (Above of below the ring), depending on with side the addition took place. (See attachment)
It is the carbon of the carbonyl in the open-chain form of the sugar, because it is the only one that can react with the Hydroxyls.
Answer:
The solution is given below.
Explanation:
Speed = Distance(m)/Time(sec.)
Distance traveled = 150 m
Time taken = 3.5 seconds
Speed of car = 150/3.5 = 42.86 m/s
So the car traveled at a speed of 42.86 m/s.
Pitch is sometimes defined as the fundamental frequency of a sound wave. For most practical purposes, this is fine, and pitch and frequency can be thought of as equivalent. On the other hand, for most practical purposes, amplitude can be thought of as volume.
However, technically, pitch and volume are human perceptions. Thus, our perception of pitch and volume are not solely based on frequency and amplitude respectively, but are based on a combination of both. Frequency overwhelming dictates perceived pitch, but amplitude also does have some small, small effect on our pitch perception, especially when it is very large. For example, a very loud sound can have a different perceived pitch than you would predict from its frequency alone.
Hope that helps!
Answer:
Draw structures corresponding to the following IUPAC names:(a) (Z)-2-Ethyl-2-buten-1-ol (b) 3-Cyclohexen-1-ol(c) trans-3-Chlorocycloheptanol (d) 1,4-Pentanediol(e) 2,6-Dimethylphenol (f ) o-(2-Hydroxyethyl)phenol
Explanation:
According to IUPAC rules, the name of a compound is:
Prefix+root word+suffix
1) Select the longest carbon chain and it gives the root word.
2) The substituents give the prefix.
3) The functional group gives the secondary suffix and the type of carbon chain gives the primary suffix.
The structure of the given compounds are shown below: