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There actually are SIMPLE... Bubbling ozone thorough a solution of 2-butene and methanol at a temperature of -78°C will give you an ozonide, which on REDUCTION with zinc will PRODUCE two moles of ethanal. Reducing ethanal with LITHIUM aluminum HYDRIDE and hydrolysing will produce ethanol.KEEP SMILING...MARK AS BRAINLIST..

I THINK its 3. that is 3×10²³ CARBON atomscheck it once I am not CONFIDENT

The SALT X is CUCO3(COPPER CARBONATE).

i-Na=Reducing,O=Oxidising agentii-CuO=Oxidising,H=Reducing AGENT

In Hex−1−en−3−ol PARENT chain has 6 carbons. The first carbon has double bond. The third carbon has alcohol −OH functional GROUP as substituent. SEE the attached image, that may help you¶ THANK YOU ¶PLEASE MARK AS BRAINLIEST ~~~^^

tion:Structure in the attachment ADDITIONAL information :-Full form of IUPAC :-International union of PURE and applied chemistry The number of carbon ATOMS in a hydrocarbon is indicated by using the following stems :For 1 carbon it is indicated by MethFor 2 carbon it is indicated by EthFor 3 carbon it is indicated by propFor 4 carbon it is indicated by but For 5 carbon it is indicated by pentA saturated hydrocarbon containing single bonds is indicated by - ane. An unsaturated hydrocarbon containing double bonds is indicated by - ene. An unsaturated hydrocarbon containing triple bonds is indicated by - yne.

tion:2-methyl-2-propen-1-olAdditional information :-FULL form of IUPAC :-International union of pure and applied CHEMISTRY The number of carbon atoms in a hydrocarbon is indicated by using the FOLLOWING stems :For 1 carbon it is indicated by MethFor 2 carbon it is indicated by EthFor 3 carbon it is indicated by propFor 4 carbon it is indicated by but For 5 carbon it is indicated by pentA saturated hydrocarbon containing single bonds is indicated by - ANE. An unsaturated hydrocarbon containing double bonds is indicated by - ene. An unsaturated hydrocarbon containing TRIPLE bonds is indicated by - yne.

butan-2-ol is the IUPAC NAME of this COMPOUND

tion:1-phenyl-2-propanolAdditional information :-Full FORM of IUPAC :-INTERNATIONAL union of pure and applied chemistry The number of carbon atoms in a hydrocarbon is indicated by using the FOLLOWING stems :For 1 carbon it is indicated by MethFor 2 carbon it is indicated by EthFor 3 carbon it is indicated by propFor 4 carbon it is indicated by but For 5 carbon it is indicated by pentA saturated hydrocarbon containing single bonds is indicated by - ane. An UNSATURATED hydrocarbon containing double bonds is indicated by - ene. An unsaturated hydrocarbon containing triple bonds is indicated by - yne.

tion:2,2-Dimethylpropan-1-ol Additional information :-FULL form of IUPAC :-International union of pure and applied chemistry The number of carbon ATOMS in a hydrocarbon is indicated by using the following STEMS :For 1 carbon it is indicated by MethFor 2 carbon it is indicated by EthFor 3 carbon it is indicated by propFor 4 carbon it is indicated by but For 5 carbon it is indicated by pentA SATURATED hydrocarbon containing single bonds is indicated by - ane. An unsaturated hydrocarbon containing double bonds is indicated by - ENE. An unsaturated hydrocarbon containing triple bonds is indicated by - yne.

tion:4-hexen-3-olAdditional information :-Full form of IUPAC :-International union of pure and APPLIED CHEMISTRY The number of carbon atoms in a hydrocarbon is indicated by using the following STEMS :For 1 carbon it is indicated by MethFor 2 carbon it is indicated by EthFor 3 carbon it is indicated by propFor 4 carbon it is indicated by but For 5 carbon it is indicated by pentA saturated hydrocarbon containing SINGLE bonds is indicated by - ane. An unsaturated hydrocarbon containing double bonds is indicated by - ene. An unsaturated hydrocarbon containing triple bonds is indicated by - yne.

tion:2-methyl-propan-1,3-diolAdditional INFORMATION :-Full form of IUPAC :-International union of pure and applied chemistry The number of carbon atoms in a HYDROCARBON is indicated by USING the following stems :For 1 carbon it is indicated by MethFor 2 carbon it is indicated by EthFor 3 carbon it is indicated by propFor 4 carbon it is indicated by butFor 5 carbon it is indicated by pentA saturated hydrocarbon CONTAINING single bonds is indicated by - ANE. An unsaturated hydrocarbon containing double bonds is indicated by - ene. An unsaturated hydrocarbon containing triple bonds is indicated by - yne.

3-methyl-but-2-en-1-ol is the IUPAC NAME of this COMPOUND

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It is a SINGLE replacement reaction where zinc metal displaces the hydrogen to form hydrogen GAS and zinc chloride, a salt. Zinc REACTS QUICKLY with the acid to form bubbles of hydrogen. Explanation: the metal zinc reacts with hydrochloric acid it PRODUCE hydrogen gas and zinc chloride.

Nitrogen gasExplanation:because it PREVENTS to OXIDATION with air and prevents stale noss of chips so they USE air ALONG with nitrogen GAS

Explanation:      0.1 N SODIUM CARBONATE SOLUTION, HOW TO PREPARE SODIUM CARBONATE IN LABORATORY, HOW TO PREPARE SODIUM CARBONATE SOLUTION IN LABORATORY, MOLAR SOLUTION, MORLARITY, NORMAL SOLUTION, NORMALITY, PREPARATION OF SOLUTION, SODIUM CARBONATE SOLUTION, STANDARDIZED SOLUTIONA solution is a homogeneous mixture COMPOSED of only one phase. In such a mixture, a solute is a substance dissolved in another substance called as the solvent. The concentration of a solute in a solution is a measure of how MUCH of that solute is dissolved in a solvent.Standard SOLUTIONS are those in which the exact amount of a substance presents in a definite volume of solution. To prepare the standard solution, a known WEIGHT of solute is measured on a well-calibrated weighing scale and then dissolved in a solvent (usually distilled water) to make up a specific volume.

100grams of glucose NEED to be burned to PRODUCE 8354 kj of HEAT

i THINK it MAY DECREASE

Explanation:Phenols give o- and p-nitrophenol on nitration with CONC. HNO3 and H2SO4 mixture. —OH group in PHENOL is o–, p– directing. phenols-give-o-and-p-nitrophenol-on-nitration-with-conc-hno3-and-h2so4-mixture

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Explanation:            In p-nitrophenol, MOLECULAR association takes PLACE due to extensive hydrogen bonding between the molecules (intermolecular hydrogen bonding). Therefore, it has higher MELTING and boiling points. In o-nitrophenol, since the OH and NO2 are in close proximity to each other, intramolecular hydrogen bonding takes place.

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the VALUE of Z is BENZOL

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Ammonium CARBONATE belongs to the class of organic compounds known as organic CARBONIC ACIDS. Organic carbonic acids are compounds comprising the carbonic acid functional group. Ammonium carbonate is a very weakly acidic COMPOUND (based on its PKA)

Explanation:2NaoH+Zn ———>Na2Zno2+H2

ur answerThe OXIDATION NUMBER of NITROGEN in dinitrogen pentoxide is 5....

ionic bond ........is formed between an element of GROUP 1,A and VII A of the periodic table

Explanation:A polymer is a large molecule, or macromolecule, composed of many repeated subunits.[6] Due to their broad range of properties,[7] both synthetic and NATURAL polymers play essential and ubiquitous roles in everyday life.[8] Polymers range from familiar synthetic plastics such as polystyrene to natural biopolymers such as DNA and proteins that are fundamental to biological structure and function. Polymers, both natural and synthetic, are created via polymerization of many small molecules, known as monomers. Their consequently large molecular mass, relative to small molecule compounds, produces unique physical properties including toughness, viscoelasticity, and a tendency to form glasses and semicrystalline structures rather than crystals. The terms polymer and resin are often synonymous with plastic. The term "polymer" derives from the Greek word πολύς (polus, meaning "many, much") and μέρος (meros, meaning "part"), and refers to a molecule whose structure is composed of multiple repeating units, from which originates a characteristic of high relative molecular mass and attendant properties.[3] The units composing polymers derive, actually or CONCEPTUALLY, from molecules of low relative molecular mass.[3] The term was coined in 1833 by Jöns Jacob Berzelius, though with a definition distinct from the modern IUPAC definition.[9][10] The modern concept of polymers as covalently bonded macromolecular structures was proposed in 1920 by Hermann Staudinger,[11] who spent the NEXT decade finding experimental evidence for this HYPOTHESIS.[12] Polymers are studied in the FIELDS of biophysics and macromolecular science, and polymer science (which includes polymer chemistry and polymer physics). Historically, products arising from the linkage of repeating units by covalent chemical bonds have been the primary focus of polymer science; emerging important areas of the science now focus on non-covalent links. Polyisoprene of latex rubber is an example of a biological polymer, and the polystyrene of styrofoam is an example of a synthetic polymer. In biological contexts, essentially all biological macromolecules—i.e., proteins (polyamides), nucleic acids (polynucleotides), and polysaccharides—are purely polymeric, or are composed in large part of polymeric components—e.g., isoprenylated or lipid-modified glycoproteins, where small lipidic molecules and oligosaccharide modifications occur on the polyamide backbone of the protein.[13

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