1 4 di tert butyl 2 5 dimethoxybenzene. 1,4 2022-10-23

1 4 di tert butyl 2 5 dimethoxybenzene Rating: 7,8/10 1287 reviews

1,4-Di-tert-butyl-2,5-dimethoxybenzene is a chemical compound with the molecular formula C16H24O2. It is a derivative of benzene, a six-carbon aromatic hydrocarbon, with two tert-butyl groups and two methoxy groups attached to the aromatic ring. Tert-butyl groups are carbon-based substituents with the formula (CH3)3C-, while methoxy groups are oxygen-containing substituents with the formula -OCH3.

1,4-Di-tert-butyl-2,5-dimethoxybenzene is a white solid at room temperature, with a melting point of approximately 40-41°C and a boiling point of approximately 250-252°C. It is soluble in a variety of organic solvents, including ethanol, ether, and acetone, but is insoluble in water.

The chemical properties of 1,4-di-tert-butyl-2,5-dimethoxybenzene are largely determined by the presence of the aromatic ring and the substituents attached to it. The aromatic ring is a planar, six-membered ring of carbon atoms bonded together by alternating double bonds. It is characterized by its high degree of stability, due to the delocalization of electrons within the ring, and is responsible for the chemical reactivity of aromatic compounds. The tert-butyl and methoxy groups are electron-withdrawing substituents, meaning that they tend to stabilize the aromatic ring by withdrawing electron density from it. This can affect the reactivity of the compound, as well as its physical properties, such as its solubility and melting point.

1,4-Di-tert-butyl-2,5-dimethoxybenzene has a number of potential uses in a variety of fields. It has been investigated as a potential antioxidant, due to its ability to inhibit the oxidation of unsaturated fatty acids, and as a corrosion inhibitor, due to its ability to form a protective film on metal surfaces. It has also been studied as a potential component of resins and polymers, due to its ability to improve the mechanical and thermal properties of these materials.

In conclusion, 1,4-di-tert-butyl-2,5-dimethoxybenzene is a chemical compound with a unique set of properties and potential uses. Its aromatic ring and substituents give it a range of physical and chemical properties that make it a useful compound in a variety of applications.

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1 4 di tert butyl 2 5 dimethoxybenzene

P352 Wash with plenty of soap and water. P304 + P340 IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. P244 Keep reduction valves free from grease and oil. P411 + P235 Keep cool. P374 Fight fire with normal precautions from a reasonable distance. P103 Read label before use Prevention Code Phrase P201 Obtain special instructions before use. P403 Store in a well-ventilated place.

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1 4 di tert butyl 2 5 dimethoxybenzene

P341 If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. P285 In case of inadequate ventilation wear respiratory protection. Oxidising gases section 2. P403 + P233 Store in a well-ventilated place. Fight fire remotely due to the risk of explosion. P272 Contaminated work clothing should not be allowed out of the workplace. P230 Keep wetted P231 Handle under inert gas.

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1 4 di tert butyl 2 5 dimethoxybenzene

The dimethoxybenzene contains two activating methoxy groups, which are ortho, para directors. P362 Take off contaminated clothing and wash before reuse. The reaction was then allowed to go to completion at room temperature, and the crystals were washed with water and methanol. P223 Keep away from any possible contact with water, because of violent reaction and possible flash fire. This is true of aromatic compounds, meaning they are stable. P262 Do not get in eyes, on skin, or on clothing. Storage Code Phrase P401 P402 Store in a dry place.

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1 4 di tert butyl 2 5 dimethoxybenzene

P381 Eliminate all ignition sources if safe to do so. P335 Brush off loose particles from skin. P233 Keep container tightly closed. This gives a total of 4n+2 π electrons. P264 Wash hands thoroughly after handling. P370 + P380 + P375 In case of fire: Evacuate area. P221 Take any precaution to avoid mixing with combustibles P222 Do not allow contact with air.

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1 4 di tert butyl 2 5 dimethoxybenzene

P331 Do NOT induce vomiting. P370 In case of fire: P371 In case of major fire and large quantities: P372 Explosion risk in case of fire. The actual yield of the product is 0. According to Hückel's Molecular Orbital Theory , a compound is particularly stable if all of its bonding molecular orbitals are filled with paired electrons. P102 Keep out of reach of children. These 4 fill in the orbitals of the succeeding energy level 2.

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1 4 di tert butyl 2 5 dimethoxybenzene

The preparation of the 1,4-di- tert -butyl- 2,5- dimethoxybenzene was overall successful when the data is evaluated. If the compound does not meet all the following criteria, it is likely not aromatic. Do not rub affected area. With aromatic compounds, 2 electrons fill the lowest energy molecular orbital, and 4 electrons fill each subsequent energy level the number of subsequent energy levels is denoted by n , leaving all bonding orbitals filled and no anti-bonding orbitals occupied. P301 + P330 + P331 IF SWALLOWED: Rinse mouth. P404 Store in a closed container.

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1 4 di tert butyl 2 5 dimethoxybenzene

P306 + P360 IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes. P321 P322 P330 Rinse mouth. P410 + P403 Protect from sunlight. P320 P302 + P352 IF ON SKIN: wash with plenty of soap and water. P410 + P412 Protect from sunlight. Store in a well-ventilated place. P302 + P350 IF ON SKIN: Gently wash with plenty of soap and water.

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1 4 di tert butyl 2 5 dimethoxybenzene

P235 + P410 Keep cool. P363 Wash contaminated clothing before reuse. Benzene has 6 π electrons. P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Normal substitution of an aromatic ring does not occur because of the stability of the ring 2. P273 Avoid release to the environment. P336 Thaw frosted parts with lukewarm water.


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