Answer:
It allows the wheels to move of the neutral position without the tires scrubbing
Explanation:
The double wishbone suspension is independent and it can be used in both the front wheels and it affords very good control of the outward or inward tilting of the front wheel and it keeps the wheels perpendicular to the road surface
However, when equal length parallel wishbone are installed, it gives rise to scrubbing of the tires as the wheels turn in the tracks
The development of unequal length non-parallel transverse or converging wishbones with A-arms suspension resolved the tire scrubbing effect on the wheels when moving out of the neutral position.
Same question idea but different values... I hope I helped you... Don't forget to put a heart mark
B. Always cut away from the body
Answer:
See detailed explanation and image attached
Explanation:
1 mole of 1-pentanol reacts with 1 mole of benzhydrol
Number of moles in 1.5 g of benzhydrol = mass/molar mass = 1.5 g/184 g/mol = 0.008 moles of benzhydrol
x moles of 1-pentanol reacts with 0.008 moles of benzhydrol
x = 0.008 moles of 1-pentanol
If 1 mole occupies 22.4 L
0.008 moles occupies 22.4 * 0.008 moles = 0.179 L of 1-pentanol is required.
The mechanism of the formation of n-pentyl benzhydryl ether involves the protonation of the -OH group in benzhydrol. This is followed by loss of water molecule creating a carbocation which is attacked by the 1-pentanol. Abstraction of a proton by a base completes the mechanism, regenerates the acid and yields the n-pentyl benzhydryl ether as shown in the image attached.
The synthesis of diethyl ether occurs by protonation of one ethanol molecule followed by SN2 attack by anothe ethanol molecule and a simultaneous loss of a water molecule. Deprotonation by a base yields the diethyl ether